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Journal of Thrombosis and Haemostasis : JTH|October 21, 2016
Immunochip analysis identifies novel susceptibility loci in the human leukocyte antigen region for acquired thrombotic thrombocytopenic purpuraI Mancini, I Ricaño-Ponce, E Pappalardo, et al.
Human Molecular Genetics|May 1, 1993
No evidence of genetic heterogeneity in Brazilian facioscapulohumeral muscular dystrophy families (FSHD) with 4q markersM R Passos-Bueno, C Wijmenga, R E Takata, et al.
Molecular Psychiatry|September 26, 2007
An association screen of myelin-related genes implicates the chromosome 22q11 PIK4CA gene in schizophreniaB J Jungerius, M L C Hoogendoorn, S C Bakker, et al.
Nature Genetics|September 1, 1992
Chromosome 4q DNA rearrangements associated with facioscapulohumeral muscular dystrophyC Wijmenga, J E Hewitt, L A Sandkuijl, et al.
Human Molecular Genetics|August 1, 1994
Analysis of the tandem repeat locus D4Z4 associated with facioscapulohumeral muscular dystrophyJ E Hewitt, R Lyle, L N Clark, et al.
The Journal of Clinical Endocrinology and Metabolism|May 3, 2003
A genome-wide scan in type 2 diabetes mellitus provides independent replication of a susceptibility locus on 18p11 and suggests the existence of novel Loci on 2q12 and 19q13J H O van Tilburg, L A Sandkuijl, E Strengman, et al.
Muscle & Nerve. Supplement|January 1, 1995
Search for the FSHD gene using cDNA selection in a region spanning 100 kb on chromosome 4q35J C van Deutekom, M H Hofker, S Romberg, et al.
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