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Acta Neuropathologica Communications|October 3, 2014
Abundant kif21b is associated with accelerated progression in neurodegenerative diseasesKarim L Kreft, Marjan van Meurs, Annet F Wierenga-Wolf, et al.Experimental Neurology|September 30, 2006
Audiogenic seizure susceptibility is reduced in fragile X knockout mice after introduction of FMR1 transgenesSebastiano A Musumeci, Giuseppe Calabrese, Carmela M Bonaccorso, et al.American Journal of Medical Genetics. Part A|August 12, 2003
Isolated postaxial polydactyly type B with mosaicism of a submicroscopic unbalanced translocation leading to an extended phenotype in offspringRobert-Jan H Galjaard, Herma C van der Linde, Bert H J Eussen, et al.American Journal of Medical Genetics|August 9, 1996
Transgenic mouse model for the fragile X syndromeR F Kooy, R D'Hooge, E Reyniers, et al.Journal of Medical Genetics|September 1, 1993
Clinical and molecular studies in fragile X patients with a Prader-Willi-like phenotypeB B de Vries, J P Fryns, M G Butler, et al.Human Molecular Genetics|May 7, 2004
Fxr1 knockout mice show a striated muscle phenotype: implications for Fxr1p function in vivoEdwin J Mientjes, Rob Willemsen, Laura L Kirkpatrick, et al.American Journal of Medical Genetics|April 1, 1992
Characterization of a highly polymorphic dinucleotide repeat 150 KB proximal to the fragile X siteG J Riggins, S L Sherman, B A Oostra, et al.Journal of Medical Genetics|December 10, 1997
Prenatal diagnosis of the fragile X syndrome: loss of mutation owing to a double recombinant or gene conversion event at the FMR1 locusM Losekoot, E Hoogendoorn, R Olmer, et al.European Journal of Human Genetics : EJHG|May 8, 2003
A new locus for postaxial polydactyly type A/B on chromosome 7q21-q34Robert-Jan H Galjaard, Arie P T Smits, Joep H A M Tuerlings, et al.European Journal of Human Genetics : EJHG|September 26, 2001
X-linked recessive inheritance of radial ray deficiencies in a family with four affected malesR J Galjaard, N Kostakoglu, J J Hoogeboom, et al.Pageof 51