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Human Genetics|November 18, 2015
Whole-exome sequencing identifies mutations of TBC1D1 encoding a Rab-GTPase-activating protein in patients with congenital anomalies of the kidneys and urinary tract (CAKUT)Anne Kosfeld, Martin Kreuzer, Christoph Daniel, et al.Human Genetics|August 1, 1989
Prenatal diagnosis of genetic disorders in preimplantation embryos: invasive and non-invasive approachesM Adinolfi, P E PolaniHuman Genetics|August 1, 1989
Assignment of human desmin gene to band 2q35 by nonradioactive in situ hybridizationE Viegas-Péquignot, Z L Li, B Dutrillaux, et al.Human Genetics|November 25, 2015
Genetic heterogeneity in 26 infants with a hypomyelinating leukodystrophyNatsuko Arai-Ichinoi, Mitsugu Uematsu, Ryo Sato, et al.Human Genetics|May 1, 1989
Cytogenetic studies on three pheochromocytomas derived from patients with von Hippel-Lindau syndromeM Kiechle-Schwarz, H P Neumann, H J Decker, et al.Human Genetics|May 1, 1989
Newborn screening by DNA analysis of dried blood spotsE M Rubin, K A Andrews, Y W KanHuman Genetics|May 1, 1989
Centromeric alpha satellite DNA amplification and translocation in an unusually large chromosome 14p+ variantS Dale, E Earle, L Voullaire, et al.Human Genetics|May 1, 1989
Amplification of satellite III DNA in an unusually large chromosome 14p+ variantE Earle, S Dale, K H ChooHuman Genetics|December 23, 1977
Nonrandom chromosome rearrangements in 27 cases of human myeloid leukemiaD Roźynkowa, J Stepień, J Kowalewski, et al.Human Genetics|June 6, 2016
Genome-wide association of familial prostate cancer cases identifies evidence for a rare segregating haplotype at 8q24.21Craig C Teerlink, Daniel Leongamornlert, Tokhir Dadaev, et al.Pageof 958