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Genomics|February 1, 1994
A YAC contig of approximately 3 Mb from human chromosome 5q31-->q33X Li, C A Wise, D Le Paslier, et al.
American Journal of Medical Genetics. Part A|January 28, 2003
Facial dysgenesis: a novel facial syndrome with chromosome 7 deletion p15.1-21.1Julie E Hoover-Fong, J Cai, C B Cargile, et al.
American Journal of Medical Genetics|July 16, 1999
Ocular anterior chamber dysgenesis in craniosynostosis syndromes with a fibroblast growth factor receptor 2 mutationK Okajima, L K Robinson, M A Hart, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 1, 1997
TCOF1 gene encodes a putative nucleolar phosphoprotein that exhibits mutations in Treacher Collins Syndrome throughout its coding regionC A Wise, L C Chiang, W A Paznekas, et al.
Cytogenetics and Cell Genetics|January 1, 1995
Localization of the human stem cell tyrosine kinase-1 gene (FLT3) to 13q12-->q13C E Carow, E Kim, A L Hawkins, et al.
American Journal of Human Genetics|August 1, 1995
Analysis of phenotypic features and FGFR2 mutations in Apert syndromeW J Park, C Theda, N E Maestri, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 13, 2006
Advancing age has differential effects on DNA damage, chromatin integrity, gene mutations, and aneuploidies in spermA J Wyrobek, B Eskenazi, S Young, et al.
Genomics|October 1, 1993
Genetic and physical mapping of the Treacher Collins syndrome locus with respect to loci in the chromosome 5q3 regionE W Jabs, X Li, M Lovett, et al.
Genomics|September 15, 1994
Human and mouse chromosomal mapping of the myeloid cell leukemia-1 gene: MCL1 maps to human chromosome 1q21, a region that is frequently altered in preneoplastic and neoplastic diseaseR W Craig, E W Jabs, P Zhou, et al.
Public Health Genomics|December 14, 2012
Genetic and lifestyle causal beliefs about obesity and associated diseases among ethnically diverse patients: a structured interview studyS C Sanderson, M A Diefenbach, S A Streicher, et al.
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