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American Journal of Human Genetics|March 1, 1994
Clinical, cytogenetic, and molecular characterization of seven patients with deletions of chromosome 22q13.3N J Nesslinger, J L Gorski, T W Kurczynski, et al.Proceedings of the National Academy of Sciences of the United States of America|January 20, 1999
The human LARGE gene from 22q12.3-q13.1 is a new, distinct member of the glycosyltransferase gene familyM Peyrard, E Seroussi, A C Sandberg-Nordqvist, et al.Genomics|May 18, 1999
TOM1 genes map to human chromosome 22q13.1 and mouse chromosome 8C1 and encode proteins similar to the endosomal proteins HGS and STAME Seroussi, D Kedra, M Kost-Alimova, et al.Human Genetics|July 29, 2000
Fine mapping of the constitutional translocation t(11;22)(q23;q11)I Tapia-Páez, K P O'Brien, M Kost-Alimova, et al.Genomics|December 28, 1999
A 1-Mb PAC contig spanning the common eliminated region 1 (CER1) in microcell hybrid-derived SCID tumorsY Yang, H Kiss, M Kost-Alimova, et al.The Journal of Investigative Dermatology|September 1, 1999
Psoriasis upregulated phorbolin-1 shares structural but not functional similarity to the mRNA-editing protein apobec-1P Madsen, S Anant, H H Rasmussen, et al.Human Genetics|December 6, 2001
Analysis of short stature homeobox-containing gene ( SHOX) and auxological phenotype in dyschondrosteosis and isolated Madelung deformityG Grigelioniene, J Schoumans, L Neumeyer, et al.Nature Genetics|January 1, 1997
Deregulation of the platelet-derived growth factor B-chain gene via fusion with collagen gene COL1A1 in dermatofibrosarcoma protuberans and giant-cell fibroblastomaM P Simon, F Pedeutour, N Sirvent, et al.Genomics|July 15, 1996
Regional localization of over 300 loci on human chromosome 22 using a somatic cell hybrid mapping panelM L Budarf, B Eckman, D Michaud, et al.Journal of Medical Genetics|June 10, 2005
Identification of novel deletion breakpoints bordered by segmental duplications in the NF1 locus using high resolution array-CGHK K Mantripragada, A-C Thuresson, A Piotrowski, et al.Pageof 7