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American Journal of Ophthalmology|June 1, 1996
Autosomal dominant central areolar choroidal dystrophy caused by a mutation in codon 142 in the peripherin/RDS geneC B Hoyng, P Heutink, L Testers, et al.Journal of Medical Genetics|June 1, 1994
Phenotypic analysis of triphalangeal thumb and associated hand malformationsJ Zguricas, P J Snijders, S E Hovius, et al.Human Genetics|March 7, 1998
Incomplete EcoRI digestion may lead to false diagnosis of fragile X syndromeK Storm, I Handig, E Reyniers, et al.Human Genetics|July 1, 1991
New distal marker closely linked to the fragile X locusT J Hulsebos, B A Oostra, S Broersen, et al.Neurobiology of Disease|October 22, 2008
Genes and pathways differentially expressed in the brains of Fxr2 knockout miceSebastiano Cavallaro, Sabrina Paratore, Francesco Fradale, et al.Human Molecular Genetics|January 1, 1995
Hotspot for deletions in the CGG repeat region of FMR1 in fragile X patientsE de Graaff, P Rouillard, P J Willems, et al.The Journal of Experimental Biology|August 25, 2004
Characterization of Fxr1 in Danio rerio; a simple vertebrate model to study costamere developmentBart Engels, Sandra van 't Padje, Lau Blonden, et al.The International Journal of Developmental Biology|June 22, 2005
Two members of the Fxr gene family, Fmr1 and Fxr1, are differentially expressed in Xenopus tropicalisLau Blonden, Sandra van 't Padje, Lies-Anne Severijnen, et al.Biochimica Et Biophysica Acta|August 2, 2002
Characterization of ZNF333, a novel double KRAB domain containing zinc finger gene on human chromosome 19p13.1Yong Tian, Guido J Breedveld, Shangzhi Huang, et al.Journal of Virology|August 1, 1986
Site-directed mutagenesis of polyomavirus middle-T antigen sequences encoding tyrosine 315 and tyrosine 250W Markland, B A Oostra, R Harvey, et al.Pageof 51