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American Journal of Human Genetics|March 1, 1986
Linkage studies of polymorphic, repeated DNA sequences in centromeric regions of human chromosomesE W Jabs, D A Meyers, W B Bias
Molecular and Cellular Probes|February 13, 2001
Polymorphisms in the Human SNAIL (SNAI1) geneK Okajima, W A Paznekas, T Burstyn, et al.
Biochemical and Biophysical Research Communications|September 23, 1997
Mouse TCOF1 is expressed widely, has motifs conserved in nucleolar phosphoproteins, and maps to chromosome 18W A Paznekas, N Zhang, T Gridley, et al.
Clinical Genetics|May 1, 1983
Two different structural abnormalities of chromosome 13 in offspring of chromosomally normal parents with two fragile sitesE H Mules, J Stamberg, E W Jabs, et al.
American Journal of Medical Genetics|November 6, 1995
Two craniosynostotic patients with 11q deletions, and review of 48 casesA F Lewanda, S Morsey, C S Reid, et al.
Methods in Molecular Biology (Clifton, N.J.)|January 1, 1997
Linkage analysis of genetic disordersE W Taylor, J Xu, E W Jabs, et al.
Clinical Genetics|June 1, 1987
Single maxillary central incisor and coloboma in hypomelanosis of ItoD W Bartholomew, E W Jabs, L S Levin, et al.
Human Genetics|March 1, 1988
Association of a new chromosomal deletion [del(1)(q32q42)] with diaphragmatic hernia: assignment of a human ferritin geneH Youssoufian, P Chance, C M Tuck-Muller, et al.
The Journal of Biological Chemistry|March 25, 1993
Cloning, overexpression, and genomic mapping of the 14-kDa subunit of human replication protein AC B Umbricht, L F Erdile, E W Jabs, et al.
Chromosoma|November 1, 1995
Human gamma X satellite DNA: an X chromosome specific centromeric DNA sequenceC Lee, X Li, E W Jabs, et al.
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