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American Journal of Medical Genetics|February 1, 1991
Multipoint linkage analysis of DXS369 and DXS304 in fragile X familiesB A van Oost, A Smits, J C Dreesen, et al.
Neurobiology of Disease|November 1, 2005
The generation of a conditional Fmr1 knock out mouse model to study Fmrp function in vivoE J Mientjes, I Nieuwenhuizen, L Kirkpatrick, et al.
Clinical Genetics|July 31, 2007
Exceptional good cognitive and phenotypic profile in a male carrying a mosaic mutation in the FMR1 geneL C P Govaerts, A E Smit, J J Saris, et al.
Lancet (London, England)|April 9, 2002
Association between genetic variation in the gene for insulin-like growth factor-I and low birthweightNorbert Vaessen, Joop A Janssen, Peter Heutink, et al.
Human Molecular Genetics|August 7, 2001
Instability of a (CGG)98 repeat in the Fmr1 promoterC J Bontekoe, C E Bakker, I M Nieuwenhuizen, et al.
Growth Hormone & IGF Research : Official Journal of the Growth Hormone Research Society and the International IGF Research Society|September 28, 2011
Common polymorphisms in the GH/IGF-1 axis contribute to growth in extremely tall subjectsA E J Hendriks, M R Brown, A M Boot, et al.
Human Molecular Genetics|April 10, 1999
Different targets for the fragile X-related proteins revealed by their distinct nuclear localizationsF Tamanini, C Bontekoe, C E Bakker, et al.
European Journal of Human Genetics : EJHG|July 10, 2008
Familial aggregation of preeclampsia and intrauterine growth restriction in a genetically isolated population in The NetherlandsAnne L Berends, Eric A Steegers, Aaron Isaacs, et al.
Psychiatric Genetics|January 7, 2009
Role of shared genetic and environmental factors in symptoms of depression and body compositionWing Chi Choy, Sandra López-León, Yurii S Aulchenko, et al.
Human Genetics|September 20, 2015
Heritabilities, proportions of heritabilities explained by GWAS findings, and implications of cross-phenotype effects on PR intervalClaudia Tamar Silva, Jan A Kors, Najaf Amin, et al.
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