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Genomics|August 1, 1992
Fine-mapping of the spinal muscular atrophy locus to a region flanked by MAP1B and D5S6L M Brzustowicz, P W Kleyn, F M Boyce, et al.
Journal of Neurodevelopmental Disorders|April 13, 2011
Novel method for combined linkage and genome-wide association analysis finds evidence of distinct genetic architecture for two subtypes of autismVeronica J Vieland, Joachim Hallmayer, Yungui Huang, et al.
Nature|August 4, 1985
Detection of deletions spanning the Duchenne muscular dystrophy locus using a tightly linked DNA segmentA P Monaco, C J Bertelson, W Middlesworth, et al.
Science (New York, N.Y.)|February 3, 1995
Association between X-linked mixed deafness and mutations in the POU domain gene POU3F4Y J de Kok, S M van der Maarel, M Bitner-Glindzicz, et al.
European Journal of Human Genetics : EJHG|October 22, 1998
Integrated physical and transcript map of 5q31.3-qterM Kostrzewa, B W Krings, M J Dixon, et al.
Neurogenetics|May 27, 2005
Identification of a VPS13A founder mutation in French Canadian families with chorea-acanthocytosisCarol Dobson-Stone, Antonio Velayos-Baeza, An Jansen, et al.
Genomics|June 10, 1995
A high-resolution interval map of the q21 region of the human X chromosomeC Philippe, C Arnould, F Sloan, et al.
Oncogene|July 30, 2008
Lipocalin 2 is required for BCR-ABL-induced tumorigenesisX Leng, H Lin, T Ding, et al.
Endoscopic Ultrasound|June 21, 2014
Transrectal ultrasound - Techniques and outcomes in the management of intestinal endometriosisLucio G B Rossini, Paulo A A G Ribeiro, Francisco C M Rodrigues, et al.
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