Showing results (1601-1610 of 5,631) with videos related to

Sort By:
Pageof 564
European Journal of Human Genetics : EJHG|October 28, 2004
Supernumerary marker chromosomes in man: parental origin, mosaicism and maternal age revisitedJohn A Crolla, Sheila A Youings, Sarah Ennis, et al.
European Journal of Human Genetics : EJHG|September 16, 2004
An excess of chromosome 1 breakpoints in male infertilityIben Bache, Elvire Van Assche, Sultan Cingoz, et al.
European Journal of Human Genetics : EJHG|October 16, 2004
Delineation of mechanisms and regions of dosage imbalance in complex rearrangements of 1p36 leads to a putative gene for regulation of cranial suture closureMarzena Gajecka, Wei Yu, Blake C Ballif, et al.
European Journal of Human Genetics : EJHG|October 16, 2004
Mutations including the promoter region of myocilin/TIGR geneMaria Saura, Montse Cabana, Carmen Ayuso, et al.
European Journal of Human Genetics : EJHG|November 13, 2004
Quantification of allele-specific G-protein beta3 subunit mRNA transcripts in different human cells and tissues by PyrosequencingAijun Sun, Junbo Ge, Winfried Siffert, et al.
European Journal of Human Genetics : EJHG|September 2, 2004
Extension of the mutation spectrum in Friedreich's ataxia: detection of an exon deletion and novel missense mutationsC H Zühlke, A Dalski, M Habeck, et al.
European Journal of Human Genetics : EJHG|November 4, 2004
Y chromosome evidence for a founder effect in Ashkenazi JewsAlmut Nebel, Dvora Filon, Marina Faerman, et al.
European Journal of Human Genetics : EJHG|November 4, 2004
Mutations in the known genes are not the major cause of MED; distinctive phenotypic entities among patients with no identified mutationsEveliina Jakkula, Outi Mäkitie, Malwina Czarny-Ratajczak, et al.
European Journal of Human Genetics : EJHG|November 4, 2004
Haplotype structure of the beta adrenergic receptor genes in US Caucasians and African AmericansInna Belfer, Beata Buzas, Catherine Evans, et al.
European Journal of Human Genetics : EJHG|October 21, 2004
Microarray-based mutation analysis of the ABCA4 (ABCR) gene in autosomal recessive cone-rod dystrophy and retinitis pigmentosaB Jeroen Klevering, Suzanne Yzer, Klaus Rohrschneider, et al.
Pageof 564