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Journal of Human Genetics|March 20, 1999
Clinical applications of two-color telomeric fluorescence in situ hybridization for prenatal diagnosis: identification of chromosomal translocation in five families with recurrent miscarriages or a child with multiple congenital anomaliesK Wakui, M Tanemura, K Suzumori, et al.Journal of Human Genetics|March 20, 1999
Ret/PTC3 is the most frequent form of gene rearrangement in papillary thyroid carcinomas in JapanY Kitamura, K Minobe, T Nakata, et al.Journal of Human Genetics|March 20, 1999
A novel nonsense mutation of the PEX7 gene in a patient with rhizomelic chondrodysplasia punctataN Shimozawa, Y Suzuki, Z Zhang, et al.Journal of Human Genetics|March 20, 1999
Chromosomal assignment of a human apoptosis-associated tyrosine kinase gene on chromosome 17q25.3 by somatic hybrid analysis and fluorescence in situ hybridizationN Seki, A Hayashi, A Hattori, et al.Journal of Human Genetics|April 3, 2001
Analysis for microdeletions of Y chromosome in a single spermatozoon from a man with severe oligozoospermiaS Komori, Y Nakata, K Sakata, et al.Journal of Human Genetics|April 3, 2001
Y chromosome compound haplotypes with the microsatellite markers DXYS265, DXYS266, and DXYS241J Lee, S E Kotliarova, A A Ewis, et al.Journal of Human Genetics|February 24, 2001
A novel mutation in a family with non-erythroid variant form of acute intermittent porphyriaS Yu, V Poulos, P StewartJournal of Human Genetics|February 24, 2001
Molecular cloning of a novel human gene (SIRP-B2) which encodes a new member of the SIRP/SHPS-1 protein familyY Ichigotani, S Matsuda, K Machida, et al.Journal of Human Genetics|March 4, 2000
cDNA cloning of a novel human gene NAKAP95, neighbor of A-kinase anchoring protein 95 (AKAP95) on chromosome 19p13.11-p13.12 regionN Seki, N Ueki, K Yano, et al.Journal of Human Genetics|March 4, 2000
A family with hydrocephalus as a complication of cerebellar hemangioblastoma: identification of Pro157Leu mutation in the VHL geneK Fukino, A Teramoto, K Adachi, et al.Pageof 351