Academic bibliography for
Kooy Frank (91)
- Article (83)
- Book chapter (4)
- Conference proceeding (1)
- Letter to the editor (3)
The author belongs to the following faculty/faculties:
There are publications for:
2012
Article2011
Letter to the editor-
Jacquemont Sébastien, Reymond Alexandre, Zufferey Flore, Kooy Frank, Blaumeiser Bettina, Van der Aa Nathalie, et al. .- Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus
Article2010
Letter to the editor-
Walters R.G., Blaumeiser Bettina, Kooy Frank, et al. .- A new highly penetrant form of obesity due to deletions on chromosome 16p11.2
Article2009
Article-
Vandeweyer Geert, Kooy Frank.- Balanced translocations in mental retardation
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d' Hulst Charlotte, Heulens Inge, Brouwer Judith R., Willemsen Rob, de Geest Natalie, Reeve Simon P., de Deyn Peter Paul, Hassan Bassem A., Kooy Frank.- Expression of the GABAergic system in animal models for fragile X syndrome and fragile X associated tremor/ataxia syndrome (FXTAS)
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Van der Aa Nathalie, Rooms Liesbeth, Vandeweyer Geert, Ceulemans Berten, Kooy Frank, et al. .- Fourteen new cases contribute to the characterization of the 7q11.23 microduplication syndrome
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d' Hulst Charlotte, Kooy Frank.- Fragile X syndrome: from molecular genetics to therapy
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van Bon B.W.M., Vandeweyer Geert, Kooy Frank, Van der Aa Nathalie, et al. .- Further delineation of the 15q13 microdeletion and duplication syndromes: a clinical spectrum varying from non-pathogenic to a severe outcome
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Li W., Duan R., Kooy Frank, Sherman S.L., Zhou W., Jin P..- Germline mutation of microRNA-125a is associated with breast cancer
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d' Hulst Charlotte, Atack John R., Kooy Frank.- The complexity of the GABA_{A} receptor shapes unique pharmacological profiles
Book chapter-
Kooy Frank.- Fragile sites and human disease
2008
Article-
van Bon B.M.W., Koolen D.A., Borgatti R., Rooms Liesbeth, Kooy Frank, et al. .- Clinical and molecular characteristics of 1qter microdeletion syndrome: delineating a critical region for corpus callosum agenesis/hypogenesis
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Errijgers Vanessa, Fransen Erik, d' Hooge Rudi, de Deyn Peter Paul, Kooy Frank.- Effect of genetic background on acoustic startle response in fragile X knockout mice
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Kwakowsky Andrea, Schwirtlich Marija, Kooy Frank, Abrahám István, Máté Zoltán, Katarova Zoya, Szabó Gábor.- GABA neurotransmitter signaling in the developing mouse lens: dynamic regulation of components and functionality
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Koolen David A., Sistermans Erik A., Nilessen Willy, Kooy Frank, Rooms Liesbeth, et al. .- Identification of non-recurrent submicroscopic genome imbalances: the advantage of genome-wide microarrays over targeted approaches
2007
Article-
Errijgers V., van Dam D., Gantois I., van Ginneken Christa, Grossman A.W., d' Hooge Rudi, de Deyn Peter Paul, Kooy Frank.- FVB.129P2-Pde6b^{+}Tyr^{c-ch}/Ant, a sighted variant of the FVB/N mouse strain suitable for behavioral analysis
Genes, brain and behavior - ISSN 1601-1848 - 6(2007), p. 552-557
[c:irua:65066]
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Courtens Winnie, Wauters Jan, Wojciechowski Marek, Reyniers Edwin, Scheers Stefaan, van Luijk Rob, Rooms Liesbeth, Kooy Frank, Wuyts Wim.- A de novo subtelomeric monosomy 11q (11q24.2-qter) and trimosy 20q (20q13.3-qter) in a girl with findings compatible with Jacobsen syndrome: case report and review
Clinical dysmorphology - ISSN 0962-8827 - 16:4(2007), p. 231-239
[c:irua:66641]
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Lirussi Frédéric, Jonard Laurence, Gaston Véronique, Sanlaville Damien, Kooy Frank, Winnepenninckx Birgitta, Maher Eammon R., FitzPatrick David R., Gicquel Christine, Portnoï Marie-France, Couderc Rémy, Vazquez Marie-Paule, Bahuau Michel.- Beckwith-Wiedemann-like macroglossia and 18q23 haploinsufficiency
American journal of medical genetics: part A - ISSN 1552-4825 - 143:23(2007), p. 2796-2803
[c:irua:68989]
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Winnepenninckx Birgitta, Debacker Kim, Ramsay Jacqueline, Smeets Dominique, Smits Arie, FitzPatrick David R., Kooy Frank.- CGG-repeat expansion in the **DIP2B** gene is associated with the fragile site FRA12A on chromosome 12q13.1
The American journal of human genetics - ISSN 0002-9297 - 80(2007), p. 221-231
[c:irua:63005]
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Poot Martin, Kroes Hester Y., van de Wijst Suzanne E., Eleveld Marc J., Rooms Liesbeth, Nievelstein Rutger A.J., Weghuis Daniel Olde, Vreuls René C., Hageman Gerard, Kooy Frank, Hochstenbach Ron.- Dandy-Walker complex in a boy with a 5 Mb deletion of region 1q44 due to a paternal t(1;20)(q44;q13.33)
American journal of medical genetics: part A - ISSN 1552-4825 - 143:10(2007), p. 1038-1044
[c:irua:63981]
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Rooms Liesbeth, Reyniers Edwin, Kooy Frank.- Diverse chromosome breakage mechanisms underlie subtelomeric rearrangements, a common cause of mental retardation
Human mutation - ISSN 1059-7794 - 28:2(2007), p. 177-182
[c:irua:62599]
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Debacker Kim, Winnepenninckx Birgitta, Ben-Porat Neta, FitzPatrick David, van Luijk Rob, Scheers Stefaan, Kerem Batsheva, Kooy Frank.- FRA18C, a new aphidicolin inducable fragile site on chromosome 18q22, possibly associated with in vivo chromosome breakage
Journal of medical genetics - ISSN 0022-2593 - 44(2007), p. 347-352
[c:irua:63625]
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Debacker Kim, Kooy Frank.- Fragile sites and human-disease
Human molecular genetics - ISSN 0964-6906 - 16:special issue 2(2007), p. R150-R158
[c:irua:66989]
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Balikova Irina, Menten Björn, de Ravel Thomy, Le Caignec Cédric, Thienpont Bernard, Urbina Montse, Doco-Fenzy Martine, de Rademaeker Marjan, Mortier Geert, Kooy Frank, van den Ende Janneke, Devriendt Koen, Fryns Jean-Pierre, Speleman Frank, Vermeesch Joris Robert.- Subtelomeric imbalances in phenotypically normal individuals
Human mutation - ISSN 1059-7794 - 28:10(2007), p. 958-967
[c:irua:63982]
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d' Hulst Charlotte, Kooy Frank.- The GABA_{A} receptor: a novel target for treatment of fragile X?
Trends in neurosciences - ISSN 0166-2236 - 30:8(2007), p. 425-431
[c:irua:65067]
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Debacker K., Winnepenninckx Birgitta, Longman C., Colgan J., Tolmie J., Murray R., van Luijk R., Scheers S., FitzPatrick D., Kooy Frank.- The molecular basis of the folate-sensitive fragile site FRA11A at 11q13
Cytogenetic and genome research - ISSN 1424-8581 - 119(2007), p. 9-14
[c:irua:68990]
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Lenski Claus, Kooy Frank, Reyniers Edwin, Loessner Daniela, Wanders Ronald J.A., Winnepenninckx Birgitta, Hellebrand Heide, Engert Stefanie, Schwartz Charles E., Meindl Alfons, Ramser Juliane.- The reduced expression of the HADH2 protein causes X-linked mental retardation, choreoathetosis, and abnormal behavior
The American journal of human genetics - ISSN 0002-9297 - 80:2(2007), p. 372-377
[c:irua:63015]
2006
Article-
Courtens Winnie, Wuyts Wim, Scheers Stefaan, van Luijk Rob, Reyniers Edwin, Rooms Liesbeth, Ceulemans Berten, Kooy Frank, Wauters Jan.- A de novo subterminal trisomy 10p and monosomy 18q in a girl with MCA/MR: case report and review
European journal of medical genetics - ISSN 1769-7212 - 49:5(2006), p. 402-413
[c:irua:56746]
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Koolen David A., Vissers Lisenka E.L.M., Pfundt Rolph, de Leeuw Nicole, Knight Samantha J.L., Regan Regina, Kooy Frank, Reyniers Edwin, Romano Corrado, Fichera Marco, Schinzel Albert, Baumer Alessandra, Anderlid Britt-Marie, Schoumans Jacqueline, Knoers Nine V., Geurts van Kessel Ad, Sistermans Erik A., Veltman Joris A., Brunner Han G., de Vries Bert B.A..- A new chromosome 17q21.31 microdeletion syndrome associated with a common inversion polymorphism
Nature genetics - ISSN 1061-4036 - 38:9(2006), p. 999-1001
[c:irua:59232]
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d' Hulst Charlotte, de Geest Nathalie, Reeve Simon P., van Dam Debby, de Deyn Peter Paul, Hassan Bassem A., Kooy Frank.- Decreased expression of the GABA_{A} receptor in fragile X syndrome
Brain research - ISSN 0006-8993 - 1121:1(2006), p. 238-245
[c:irua:61714]
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Gantois Ilse, Vandesompele Jo, Speleman Frank, Reyniers Edwin, d' Hooge Rudi, Severijnen Lies-Anne, Willemsen Rob, Tassone Flora, Kooy Frank.- Expression profiling suggests underexpression of the GABA_{A} receptor subunit δ in the fragile X knockout mouse model
Neurobiology of disease - ISSN 0969-9961 - 21:2(2006), p. 346-357
[c:irua:56617]
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Rooms Liesbeth, Reyniers E., Wuyts Wim, Storm K., van Luijk R., Scheers S., Wauters Jan, van den Ende Jef, Biervliet M., Eyskens F., Van Goethem Gert, Laridon A., Ceulemans Berten, Courtens Winnie, Kooy Frank.- Multiplex ligation-dependent probe amplification to detect subtelomeric rearrangements in routine diagnostics
Clinical genetics - ISSN 0009-9163 - 69:1(2006), p. 58-64
[c:irua:56466]
2005
Letter to the editorArticle-
van Bever Yolande, Rooms Liesbeth, Laridon Annick, Reyniers Edwin, van Luijk Rob, Scheers Stefaan, Wauters Jan, Kooy Frank.- Clinical report of a pure subtelomeric 1qter deletion in a boy with mental retardation and multiple anomalies adds further evidence for a specific phenotype
American journal of medical genetics: part A - ISSN 1552-4825 - 135:1(2005), p. 91-95
[c:irua:52711]
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van Dam Debby, Errijgers Vanessa, Kooy Frank, Willemsen Rob, Mientjes Edwin, Oostra Ben A., de Deyn Peter Paul.- Cognitive decline, neuromotor and behavioural disturbances in a mouse model for fragile-X-associated tremor/ataxia syndrome (FXTAS)
Behavioural brain research - ISSN 0166-4328 - 162:2(2005), p. 233-239
[c:irua:53434]
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van Laer Lut, Pfister Markus, Thys Sofie, Vrijens Karen, Mueller Marcus, Umans Lieve, Serneels Lutgarde, van Nassauw Luc, Kooy Frank, Smith Richard J.H., Timmermans Jean-Pierre, van Leuven Fred, van Camp Guy.- Mice lacking Dfna5 show a diverging number of cochlear fourth row outer hair cells
Neurobiology of disease - ISSN 0969-9961 - 19:3(2005), p. 386-399
[c:irua:53645]
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Rooms Liesbeth, Reyniers Edwin, Kooy Frank.- Subtelomeric rearrangements in the mentally retarded: a comparison of detection methods
Human mutation - ISSN 1059-7794 - 25:6(2005), p. 513-524
[c:irua:56464]
2004
Article-
Ramser J., Winnepenninckx Birgitta, Lenski C., Errijgers V., Platzer M., Schwartz C., Meindl A., Kooy Frank.- A splice site mutation in the methyltransferase gene FTSJ1 in Xp11.23 is associated with non-syndromic mental retardation in a large Belgian family (MRX9)
Journal of medical genetics - ISSN 0022-2593 - 41(2004), p. 679-683
[c:irua:49474]
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Cornish K.M., Turk J., Wilding J., Sudhalter V., Munir F., Kooy Frank, Hagerman R..- Deconstructing the attention deficit in fragile X syndrome: a developmental neuropsychological approach
Journal of child psychology and psychiatry and allied disciplines - ISSN 0021-9630 - 45(2004), p. 1042-1053
[c:irua:49386]
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Clarke N.F., Mowat D., Kooy Frank, Reyniers E., Willemsen R..- Fragile X syndrome phenotype with normal FMR1 gene studies
American journal of medical genetics - ISSN 0148-7299 - 129A(2004), p. 326-328
[c:irua:49387]
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Errijgers V., Kooy Frank.- Genetic modifiers in mice: the example of the fragile X mouse model
Cytogenetic and genome research - ISSN 1424-8581 - 105(2004), p. 448-454
[c:irua:49472]
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Lenski C., Abidi F., Meindl A., Gibson A., Platzer M., Kooy Frank, Lubs H.A., Stevenson R.E., Ramser J., Schwartz C.E..- Novel truncating mutations in the polyglutamine tract binding protein gene, PQBP-1, cause Renpenning syndrome and XLMR in another family with microcephaly
The American journal of human genetics - ISSN 0002-9297 - 74(2004), p. 777-780
[c:irua:45568]
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Rooms Liesbeth, Reyniers Edwin, van Luijk Rob, Scheers Stefaan, Wauters Jan, Kooy Frank.- Screening for subtelomeric rearrangements using genetic markers in 70 patients with unexplained mental retardation
Annales de génétique - ISSN 0003-3995 - 47(2004), p. 53-59
[c:irua:45569]
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Rooms Liesbeth, Reyniers Edwin, van Luijk Rob, Scheers Stefaan, Wauters Jan, Ceulemans Berten, van den Ende Jenneke, van Bever Yolande, Kooy Frank.- Subtelomeric deletions detected in patients with idiopathic mental retardation using multiplex ligation-dependent probe amplification (MLPA)
Human mutation - ISSN 1059-7794 - 23(2004), p. 17-21
[c:irua:45570]
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Churchill G.A., Airey D.C., Allayee H., Kooy Frank, [et al.] .- The Collaborative Cross: a community resource for the genetic analysis of complex traits
Nature genetics - ISSN 1061-4036 - 36(2004), p. 1133-1137
[c:irua:49595]
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Christophe-Hobertus C., Kooy Frank, Gecz J., Abramowicz M.J., Holinski-Feder E., Schwartz C., Christophe D..- TM4SF10 gene sequencing in XLMR patients identifies common polymorphisms but no disease-associated mutation
BMC medical genetics - ISSN 1471-2350 - 5(2004), p. 22
[c:irua:49475]
Book chapter-
Gantois I., Kooy Frank, Oostra B.A..- Fragile X-linked mental retardation
Encyclopedia of molecular cell biology and molecular medicine / Meyers, R.A. [edit.] - Weinheim, Wiley-VCH, 2004
[c:irua:45571]
2003
Article-
Nolin S.L., Brown W.T., Glicksman A., Houck G.E., Gargano A.D., Sullivan A., Biancalana V., Bröndum-Nielsen K., Hjalgrim H., Holinski-Feder E., Kooy Frank, Longshore J., Macpherson J., Mandel J.-L., Matthijs G., Rousseau F., Steinbach P., Väisänen M.-L., von Koskull H., Sherman S.L..- Expansion of the fragile X CGG repeat in females with premutation or intermediate alleles
The American journal of human genetics - ISSN 0002-9297 - 72(2003), p. 454-464
[c:irua:41771]
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Gasteiger M., Grasbon-Frodl E., Neitzel B., Kooy Frank, Holinski-Feder E..- FMR1 gene delation/reversion: a pitfall of fragile X carrier testing
Genetic testing - ISSN 1090-6576 - 7:4(2003), p. 303-308
[c:irua:43943]
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Winnepenninckx Birgitta, Rooms Liesbeth, Kooy Frank.- Mental retardation: a review of the genetic causes
The British journal of developmental disabilities - 49(2003), p. 29-44
[c:irua:41773]
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Kooy Frank.- Of mice and the fragile X syndrome
Trends in genetics - ISSN 0168-9525 - 19(2003), p. 148-154
[c:irua:41770]
2002
Article-
Abidi F.E., Holinski-Feder E., Rittinger O., Kooy Frank, Lubs H.A., Stevenson R.E., Schwartz C.E..- A novel 2-bp deletion in the TM4SF2 is associated with MRX58
Journal of medical genetics - ISSN 0022-2593 - 39(2002), p. 430-433
[c:irua:38440]
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Lossi A.-M., Laugier-Anfossi F., Depetris D., Gecz J., Gedeon A., Kooy Frank, Schwartz C., Mattei M.-G., Croquette M.-F., Villard L..- Abnormal expression of the KLF8 (ZNF741) gene in a female patient with an X-autosome translocation t (X;21) (p11.2;122.3) and non-syndromic mental retardation
Journal of medical genetics - ISSN 0022-2593 - 39(2002), p. 113-117
[c:irua:38442]
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Winnepenninckx Birgitta, Errijgers Vanessa, Reyniers Edwin, de Deyn Peter Paul, Abidi Fatima E., Schwartz Charles E., Kooy Frank.- Family MRX9 revisited: further evidence for locus heterogeneity in MRX
American journal of medical genetics - ISSN 0148-7299 - 112(2002), p. 17-22
[c:irua:40792]
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Kooy Frank.- Genetic aspects of mental retardation
European biopharmaceutical review - (2002),
[c:irua:40796]
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Winnepenninckx Birgitta, Errijgers Vanessa, Hayez-Delatte France, Reyniers Edwin, Kooy Frank.- Identification of a family with nonspecific mental retardation (MRX79) with the A140V mutation in the MECP2 gene: is there a need for routine screening?
Human mutation - ISSN 1059-7794 - 20(2002), p. 249-252
[c:irua:39909]
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Gantois Ilse, Kooy Frank.- Targeting fragile X
Genome biology - ISSN 1465-6906 - 3:5(2002),
p. 1014.1-1014.5
[c:irua:38441]
2001
Article-
Irwin S.A., Patel B., Idupulapati M., Harris J.B., Crisostomo R.A., Larsen B.P., Kooy Frank, Willems P.J., Cras Patrick, Kozlowski P.B., Swain R.A., Weiler I.J., Greenough W.T..- Abnormal dendritic spine characteristics in the temporal and visual cortices of patients with fragile-X syndrome: a quantitative examination
American journal of medical genetics - ISSN 0148-7299 - 98(2001), p. 161-167
[c:irua:35534]
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Kooy Frank, Verhoye Marleen, Lemmon Vance, van der Linden Anne-Marie.- Brain studies of mouse models for neurogenetic disorders using in vivo magnetic resonance imaging (MRI)
European journal of human genetics / European Society of Human Genetics - ISSN 1018-4813 - 9(2001), p. 153-159
[c:irua:35535]
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Winnepenninckx Birgitta, Reyniers Edwin, Bossuyt Paul, Smits Arie, Wauters Jan, Kooy Frank.- Precise mapping of the fragile site **FRA 12A** on chromosome 12q13.1
GeneScreen - ISSN 1466-920X - 1(2001), p. 131-137
[c:irua:36324]
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Gantois I., Bakker C.E., Reyniers E., Willemsen R., d' Hooge Rudi, de Deyn Peter Paul, Oostra B.A., Kooy Frank.- Restoring the phenotype of fragile X syndrome: insight from the mouse model
Current molecular medicine - ISSN 1566-5240 - 1(2001), p. 447-455
[c:irua:35556]
2000
Article-
Holinski-Feder E., Reyniers E., Uhrig S., Golla A., Wauters Jan, Kroisel P., Bossuyt P., Rost I., Jedele K., Zierler H., Schwab S., Wildenauer D., Speicher M.R., Willems P.J., Meitinger T., Kooy Frank.- Familiar mental retardation syndrome ATR-16 due to an inherited cryptic subtelomeric translocation t(3;16)(q29;p13.3)
The American journal of human genetics - ISSN 0002-9297 - 66(2000), p. 16-25
[c:irua:28807]
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Kooy Frank, Willemsen R., Oostra B.A..- Fragile X syndrome at the turn of the century
Molecular medicine today - ISSN 1357-4310 - 6(2000), p. 194-199
[c:irua:28809]
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Bakker C.E., Kooy Frank, d' Hooge Rudi, Tamanini F., Willemsen R., Nieuwenhuizen I., de Vries B.B.A., Reyniers E., Hoogeveen A.T., Willems P.J., de Deyn Peter Paul, Oostra B.A..- Introduction of a FMRI transgene in the fragile X knockout mouse
Neuroscience research communications - ISSN 0893-6609 - 26:3(2000), p. 265-277
[c:irua:28731]
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Bliss T., Errington M., Fransen Erik, Godfraind J.-M., Kauer J.A., Kooy Frank, Maness P.F., Furley A.J.W..- Long-term potentiation in mice lacking the neural cell adhesion molecule L1
Current biology - ISSN 0960-9822 - 10(2000), p. 1607-1610
[c:irua:35493]
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van Dam Debby, d' Hooge Rudi, Hauben Ehud, Reyniers Edwin, Gantois Ilse, Bakker Cathy E., Oostra Ben A., Kooy Frank, de Deyn Peter Paul.- Spatial learning, contextual fear conditioning and conditioned emotional response in Fmr1 knockout mice
Behavioural brain research - ISSN 0166-4328 - 127(2000), p. 127-136
[c:irua:32712]
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Pfeifer D., Poulat F., Holinski-Feder E., Kooy Frank, Scherer G..- The SOX8 gene is located within 700 kb of the tip of chromosome 16 and is deleted in a patient with ATR-16 syndrome
Genomics: international journal of gene mapping and nucleotide sequencing - ISSN 0888-7543 - 63(2000), p. 108-116
[c:irua:28810]
1999
Article-
Reyniers E., van Bogaert P., Peeters N., Vits L., Pauly F., Fransen Erik, van Regemorter N., Kooy Frank.- A new neurological syndrome with mental retardation, choreoathetosis, and abnormal behavior maps to chromosome Xp11
The American journal of human genetics - ISSN 0002-9297 - 65(1999), p. 1406-1412
[c:irua:28805]
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Kooy Frank, Reyniers E., Storm K., Vits L., van Velzen D., de Ruiter P.E., Brinkmann A.O., de Paepe A., Willems P.J..- CAG repeat contraction in the androgen receptor gene in three brothers with mental retardation
American journal of medical genetics - ISSN 0148-7299 - 85(1999), p. 209-213
[c:irua:25808]
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Holden J.J.A., Percy M., Allingham-Hawkins D., Brown W.T., Chiurazzi P., Fish G., Gane L., Gunter C., Hagerman R., Jenkins E.C., Kooy Frank, Lubs H.A., Murray A., Neri G., Schwartz C., Tranebjaerg L., Villard L., Willems P.J..- Eighth International Workshop on the Fragile X Syndrome and X-linked Mental Retardation, August 16-22, 1997
American journal of medical genetics - ISSN 0148-7299 - 83(1999), p. 221-236
[c:irua:25806]
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Kooy Frank, Reyniers E., Verhoye Marleen, Sijbers Jan, Bakker C.E., Oostra B.A., Willems P.J., van der Linden Anne-Marie.- Neuroanatomy of the fragile X knockout mouse brain studied using **in vivo** high resolution magnetic resonance imaging
European journal of human genetics / European Society of Human Genetics - ISSN 1018-4813 - 7(1999), p. 526-532
[c:irua:25809]
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Reyniers Edwin, Martin Jean-Jacques, Cras Patrick, van Marck Eric, Handig Ingrid, Jorens Hugo Z.J., Oostra Ben A., Kooy Frank, Willems Patrick J..- Postmortem examination of two fragile X brothers with an **FMR1** full mutation
American journal of medical genetics - ISSN 0148-7299 - 84(1999), p. 245-249
[c:irua:23702]
1998
Article-
Storm K., Handig I., Reyniers E., Oostra B.A., Kooy Frank, Willems P.J..- Incomplete **Eco**RI digestion may lead to false diagnosis of the fragile X syndrome
Human genetics - ISSN 0340-6717 - 102(1998), p. 54-56
[c:irua:20780]
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Fransen Erik, d' Hooge Rudi, van Camp Guy, Verhoye Marleen, Sijbers Jan, Reyniers Edwin, Soriano Philippe, Kamiguchi Hiroyuki, Willemsen Rob, Koekkoek Sebastiaan K.E., de Zeeuw Chris I., de Deyn Peter Paul, van der Linden Anne-Marie, Lemmon Vance, Kooy Frank, Willems Patrick J..- L1 knockout mice show dilated ventricles, vermis hypoplasia and impaired exploration patterns
Human molecular genetics - ISSN 0964-6906 - 7:6(1998), p. 999-1009
[c:irua:19540]
Conference proceeding-
Verhoye Marleen, Sijbers Jan, Kooy Frank, Reyniers E., Fransen Erik, Oostra B.A., Willems P.J., van der Linden Anne-Marie.- MRI as a tool to study brain structure from mouse models of mental retardation
Proceedings of SPIE Medical Imaging 1998: Image Processing / Hanson, Kenneth M. [edit.] - San Diego, Calif., , 1998, p. 314-320
[c:irua:21511]
Book chapter-
Kooy Frank, Oostra B.A., Willems P.J..- The fragile X syndrome and other fragile site disorders
Trinucleotide diseases and instability / Oostra, B.A. [edit.] - Berlin, Springer, 1998, p. 1-46
[c:irua:20779]
1997
ArticleBook chapter-
Kooy Frank, Oostra B.A., Willems P.J..- Molecular detection of dynamic mutations
Human genome methods / Adolph, K.W. [edit.] - S.l., CRI, 1997, p. 23-53
[c:irua:20778]
1996
Article-
Godfraind J.-M., Reyniers E., de Boulle K., d' Hooge Rudi, de Deyn Peter Paul, Bakker C.E., Oostra B.A., Kooy Frank, Willems P.J..- Long-term potentiation in the hippocampus of fragile X knockout mouse
American journal of medical genetics - ISSN 0148-7299 - 64(1996), p. 246-251
[c:irua:16708]
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Reyniers E., van Bockstaele Dirk, de Boulle K., Kooy Frank, Bakker C.E., Oostra B.A., Willems P.J..- Mean corpuscular hemoglobin is not increased in Fmr1 knockout mice
Human genetics - ISSN 0340-6717 - 97(1996), p. 49-50
[c:irua:16706]
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Reyniers E., Wolff G., Tariverdian G., de Boulle K., Storm K., Kooy Frank, Willems P.J..- Severe mental retardation and macroorchidism without mutation in the FMR1 gene
American journal of medical genetics - ISSN 0148-7299 - 64(1996), p. 408-412
[c:irua:16710]
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Kooy Frank, d' Hooge Rudi, Reyniers E., Bakker C.E., Nagels Guy, de Boulle K., Storm K., Clincke G., de Deyn Peter Paul, Oostra B.A., Willems P.J..- Transgenic mouse model for the fragile X syndrome
American journal of medical genetics - ISSN 0148-7299 - 64(1996), p. 241-245
[c:irua:16707]