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Cytogenetics and Cell Genetics|January 1, 1993
Mapping the intron-containing human hsp90 alpha (HSPCAL4) gene to chromosome band 14q32N C Vamvakopoulos, C A Griffin, A L Hawkins, et al.American Journal of Medical Genetics|May 26, 1998
Syndrome of coronal craniosynostosis with brachydactyly and carpal/tarsal coalition due to Pro250Arg mutation in FGFR3 geneJ M Graham, S R Braddock, G R Mortier, et al.Prenatal Diagnosis|December 17, 1997
Prenatal ultrasonographic and molecular diagnosis of Apert syndromeK Filkins, J F Russo, S Boehmer, et al.Cytogenetics and Cell Genetics|February 22, 2002
Fibroblast growth factor receptor 2 (FGFR2): genomic sequence and variationsR G Ingersoll, W A Paznekas, A K Tran, et al.Genomics|October 1, 1992
Chromosomal assignment of a gene encoding a new collagen type (COL15A1) to 9q21 --> q22K Huebner, L A Cannizzaro, E W Jabs, et al.Cytogenetics and Cell Genetics|January 1, 1993
Cytogenetic survey in systemic sclerosis: correlation of aneuploidy with the presence of anticentromere antibodiesE W Jabs, C M Tuck-Muller, G J Anhalt, et al.Gene|January 30, 1993
Human cDNA clones transcribed from an unusually high-molecular-weight RNA encode a new collagen chainJ C Myers, M J Sun, J A D'Ippolito, et al.Genomics|March 1, 1991
A centromere-based genetic map of the short arm of human chromosome 6H Blanché, H Y Zoghbi, E W Jabs, et al.American Journal of Human Genetics|June 1, 1986
Regional localization of DNA sequences on chromosome 21 using somatic cell hybridsM L Van Keuren, P C Watkins, H A Drabkin, et al.Human Mutation|July 29, 1999
Clinical spectrum of fibroblast growth factor receptor mutationsM R Passos-Bueno, W R Wilcox, E W Jabs, et al.Pageof 11