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Human Genetics|April 1, 1996
Ablepharon macrostomia syndrome with associated cutis laxa: possible localization to 18qJ E Pellegrino, R E Schnur, L Boghosian-Sell, et al.Genomics|July 15, 1997
The human gene ZFP161 on 18p11.21-pter encodes a putative c-myc repressor and is homologous to murine Zfp161 (Chr 17) and Zfp161-rs1 (X Chr)I Sobek-Klocke, C Disqué-Kochem, M Ronsiek, et al.Human Molecular Genetics|January 15, 1999
An 18q- syndrome breakpoint resides between the duplicated serpins SCCA1 and SCCA2 and arises via a cryptic rearrangement with satellite III DNAS G Katz, S S Schneider, A Bartuski, et al.Genomics|December 1, 1994
Regional localization of 188 sequence tagged sites on a somatic cell hybrid mapping panel for human chromosome 3R J Leach, R Chinn, B E Reus, et al.Genomics|February 15, 1996
The generation and regional localization of 303 new chromosome 5 sequence-tagged sitesD L Grady, D L Robinson, M Gersh, et al.Genome Research|December 30, 1999
An integrated physical map for the short arm of human chromosome 5E T Peterson, R Sutherland, D L Robinson, et al.Genomics|May 1, 1993
The CEPH consortium linkage map of human chromosome 13A M Bowcock, S C Gerken, R I Barnes, et al.American Journal of Human Genetics|April 1, 1995
The 18q- syndrome: analysis of chromosomes by bivariate flow karyotyping and the PCR reveals a successive set of deletion breakpoints within 18q21.2-q22.2G A Silverman, S S Schneider, H F Massa, et al.American Journal of Human Genetics|May 1, 1993
Molecular analysis of the 18q- syndrome--and correlation with phenotypeA D Kline, M E White, R Wapner, et al.Genomics|June 15, 1996
Localization of the homolog of a mouse craniofacial mutant to human chromosome 18q11 and evaluation of linkage to human CLP and CPOA J Griffith, D L Burgess, D C Kohrman, et al.Pageof 13