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Acta Diabetologica|March 15, 2012
Heritability of dietary food intake patternsLinda van den Berg, Peter Henneman, Ko Willems van Dijk, et al.Pediatric Nephrology (Berlin, Germany)|January 17, 2008
A genome search for primary vesicoureteral reflux shows further evidence for genetic heterogeneityMaria Luisa Conte, Aida M Bertoli-Avella, Bianca M de Graaf, et al.Experimental Cell Research|December 8, 2006
Elevated Fmr1 mRNA levels and reduced protein expression in a mouse model with an unmethylated Fragile X full mutationJ R Brouwer, E J Mientjes, C E Bakker, et al.Human Molecular Genetics|April 1, 1994
A deletion of 1.6 kb proximal to the CGG repeat of the FMR1 gene causes the clinical phenotype of the fragile X syndromeH Meijer, E de Graaff, D M Merckx, et al.American Journal of Human Genetics|June 12, 1999
Noninvasive test for fragile X syndrome, using hair root analysisR Willemsen, B Anar, Y De Diego Otero, et al.Human Molecular Genetics|July 3, 2003
A long-range Shh enhancer regulates expression in the developing limb and fin and is associated with preaxial polydactylyLaura A Lettice, Simon J H Heaney, Lorna A Purdie, et al.Biochemical and Biophysical Research Communications|February 15, 1993
Biochemical genetics of glycogenosis type II in Brahman cattleH A Wisselaar, M M Hermans, W J Visser, et al.Nature Genetics|January 1, 1993
A point mutation in the FMR-1 gene associated with fragile X mental retardationK De Boulle, A J Verkerk, E Reyniers, et al.The New England Journal of Medicine|November 2, 1995
The genetic basis of the reduced expression of bilirubin UDP-glucuronosyltransferase 1 in Gilbert's syndromeP J Bosma, J R Chowdhury, C Bakker, et al.Neurobiology of Aging|November 21, 2009
Cathepsin D gene and the risk of Alzheimer's disease: a population-based study and meta-analysisM Schuur, M A Ikram, J C van Swieten, et al.Pageof 51