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Neurobiology of Disease|June 24, 2008
Rescue of behavioral phenotype and neuronal protrusion morphology in Fmr1 KO miceFemke M S de Vrij, Josien Levenga, Herma C van der Linde, et al.
Diabetologia|October 8, 2008
Sex-specific genetic effects influence variation in body compositionM C Zillikens, M Yazdanpanah, L M Pardo, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 4, 2011
The LRRK2 R1441C mutation is more frequent than G2019S in Parkinson's disease patients from southern ItalyChiara Criscuolo, Anna De Rosa, Anna Guacci, et al.
Human Molecular Genetics|November 1, 1995
Normal phenotype in two brothers with a full FMR1 mutationH J Smeets, A P Smits, C E Verheij, et al.
Diabetes Care|January 14, 2010
Genetic architecture of plasma adiponectin overlaps with the genetics of metabolic syndrome-related traitsPeter Henneman, Yurii S Aulchenko, Rune R Frants, et al.
Genomics|January 1, 1990
New polymorphic DNA marker close to the fragile site FRAXAB A Oostra, P E Hupkes, L F Perdon, et al.
Neurogenetics|September 21, 2010
Novel ATP13A2 (PARK9) homozygous mutation in a family with marked phenotype variabilityLucio Santoro, Guido J Breedveld, Fiore Manganelli, et al.
Human Genetics|May 26, 2009
Linkage analysis of adult height in a large pedigree from a Dutch genetically isolated populationTatiana I Axenovich, I V Zorkoltseva, N M Belonogova, et al.
Endocrinology|January 8, 1998
Macroorchidism in FMR1 knockout mice is caused by increased Sertoli cell proliferation during testicular developmentK E Slegtenhorst-Eegdeman, D G de Rooij, M Verhoef-Post, et al.
American Journal of Medical Genetics|April 1, 1992
Intragenic probe used for diagnostics in fragile X familiesA J Verkerk, B B deVries, M F Niermeijer, et al.
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