Showing results (81-90 of 324) with videos related to
Sort By:
Pageof 33
American Journal of Human Genetics|March 1, 1991
Clinical and molecular diagnosis of Miller-Dieker syndromeW B Dobyns, C J Curry, H E Hoyme, et al.Human Molecular Genetics|May 20, 1999
Large genomic duplicons map to sites of instability in the Prader-Willi/Angelman syndrome chromosome region (15q11-q13)S L Christian, J A Fantes, S K Mewborn, et al.Molecular Medicine Today|June 22, 2000
Lissencephaly and subcortical band heterotopia: molecular basis and diagnosisR J Leventer, D T Pilz, N Matsumoto, et al.Proceedings of the National Academy of Sciences of the United States of America|December 1, 1986
Molecular cloning and chromosomal localization of human 4-beta-galactosyltransferaseM G Humphreys-Beher, B Bunnell, P vanTuinen, et al.Somatic Cell and Molecular Genetics|May 1, 1986
Human liver fatty acid binding protein gene is located on chromosome 2S H Chen, P Van Tuinen, D H Ledbetter, et al.American Journal of Medical Genetics|January 1, 1990
A de novo X;3 translocation in Rett syndromeH Y Zoghbi, D H Ledbetter, R Schultz, et al.American Journal of Human Genetics|April 1, 1992
Maternal uniparental isodisomy of chromosome 14: association with autosomal recessive rod monochromacyL Pentao, R A Lewis, D H Ledbetter, et al.Genes & Development|April 1, 1995
Tissue-specific and allele-specific replication timing control in the imprinted human Prader-Willi syndrome regionP H Gunaratne, M Nakao, D H Ledbetter, et al.American Journal of Human Genetics|October 1, 1991
Detection of deletions and cryptic translocations in Miller-Dieker syndrome by in situ hybridizationA Kuwano, S A Ledbetter, W B Dobyns, et al.Human Molecular Genetics|February 1, 1994
Imprinting analysis of three genes in the Prader-Willi/Angelman region: SNRPN, E6-associated protein, and PAR-2 (D15S225E)M Nakao, J S Sutcliffe, B Durtschi, et al.Pageof 33