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Science (New York, N.Y.)|September 30, 1994
A comprehensive human linkage map with centimorgan density. Cooperative Human Linkage Center (CHLC)J C Murray, K H Buetow, J L Weber, et al.Teratology|May 20, 1999
Analysis of select folate pathway genes, PAX3, and human T in a Midwestern neural tube defect populationD Trembath, A L Sherbondy, D C Vandyke, et al.Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|May 1, 1994
The DNA rearrangement associated with facioscapulohumeral muscular dystrophy involves a heterochromatin-associated repetitive element: implications for a role of chromatin structure in the pathogenesis of the diseaseS T Winokur, U Bengtsson, J Feddersen, et al.Human Genetics|September 1, 1993
The human skeletal muscle adenine nucleotide translocator gene maps to chromosome 4q35 in the region of the facioscapulohumeral muscular dystrophy locusC Wijmenga, S T Winokur, G W Padberg, et al.Nature Genetics|September 1, 1992
Linkage of Rieger syndrome to the region of the epidermal growth factor gene on chromosome 4J C Murray, S R Bennett, A E Kwitek, et al.Genomics|December 1, 1992
The CEPH consortium linkage map of human chromosome 2N K Spurr, S Cox, S P Bryant, et al.Nature Genetics|June 10, 1998
A novel homeobox gene PITX3 is mutated in families with autosomal-dominant cataracts and ASMDE V Semina, R E Ferrell, H A Mintz-Hittner, et al.Mammalian Genome : Official Journal of the International Mammalian Genome Society|April 1, 1995
Genetic mapping near the myd locus on mouse chromosome 8K A Mills, K D Mathews, T Scherpbier-Heddema, et al.Cell|August 26, 1998
Pitx2, a bicoid-type homeobox gene, is involved in a lefty-signaling pathway in determination of left-right asymmetryH Yoshioka, C Meno, K Koshiba, et al.American Journal of Medical Genetics|May 14, 1999
Microdeletions at chromosome bands 1q32-q41 as a cause of Van der Woude syndromeB C Schutte, A M Basart, Y Watanabe, et al.Pageof 32