Showing results (21-30 of 33) with videos related to
Sort By:
Pageof 4
Biology of Reproduction|April 25, 2001
Expression and molecular characterization of estrogen receptor alpha messenger RNA in male reproductive organs of adult goatsM M Mansour, M R Machen, B J Tarleton, et al.Prenatal Diagnosis|March 31, 2000
DNA methylation analysis with respect to prenatal diagnosis of the Angelman and Prader-Willi syndromes and imprintingC C Glenn, G Deng, R C Michaelis, et al.Biology of Reproduction|October 24, 2001
Developmental biology of uterine glandsC A Gray, F F Bartol, B J Tarleton, et al.Nature Genetics|July 1, 1992
Evidence of founder chromosomes in fragile X syndromeR I Richards, K Holman, K Friend, et al.American Journal of Medical Genetics|May 2, 1997
Down syndrome with biparental inheritance of der(14q21q) and maternally derived trisomy 21: confirmation by fluorescent in situ hybridization and microsatellite polymorphism analysisS Rajangam, R C Michaelis, G V Velagaleti, et al.American Journal of Human Genetics|October 1, 1993
Evidence that methylation of the FMR-I locus is responsible for variable phenotypic expression of the fragile X syndromeA McConkie-Rosell, A M Lachiewicz, G A Spiridigliozzi, et al.American Journal of Medical Genetics|August 9, 1996
Lack of association between mutation size and cognitive/behavior deficits in fragile X males: a brief reportG S Fisch, N Carpenter, P N Howard-Peebles, et al.American Journal of Medical Genetics|July 15, 1994
Asymmetry of methylation with FMR-1 full mutation in two 45,X/46,XX mosaic females associated with normal intellectL R Shapiro, R J Simensen, P L Wilmot, et al.Nucleic Acids Research|August 25, 1991
Molecular heterogeneity of the fragile X syndromeY Nakahori, S J Knight, J Holland, et al.American Journal of Medical Genetics|May 8, 1995
Characterization of an unbalanced de novo rearrangement by microsatellite polymorphism typing and by fluorescent in situ hybridizationJ Zhao, P L Gordon, R S Wilroy, et al.Pageof 4