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American Journal of Human Genetics|March 11, 2000
Paternal origin of FGFR2 mutations in sporadic cases of Crouzon syndrome and Pfeiffer syndromeR L Glaser, W Jiang, S A Boyadjiev, et al.American Journal of Human Genetics|March 1, 1996
FGFR2 exon IIIa and IIIc mutations in Crouzon, Jackson-Weiss, and Pfeiffer syndromes: evidence for missense changes, insertions, and a deletion due to alternative RNA splicingG A Meyers, D Day, R Goldberg, et al.The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|November 5, 1997
Testing for interaction between maternal smoking and TGFA genotype among oral cleft cases born in Maryland 1992-1996T H Beaty, N E Maestri, J B Hetmanski, et al.American Journal of Human Genetics|June 19, 1998
Genetic heterogeneity of Saethre-Chotzen syndrome, due to TWIST and FGFR mutationsW A Paznekas, M L Cunningham, T D Howard, et al.American Journal of Human Genetics|February 11, 1999
De novo alu-element insertions in FGFR2 identify a distinct pathological basis for Apert syndromeM Oldridge, E H Zackai, D M McDonald-McGinn, et al.Gene|June 16, 2000
Cloning and chromosomal localization of the human BARX2 homeobox protein geneA Krasner, L Wallace, A Thiagalingam, et al.American Journal of Medical Genetics|June 22, 1999
Severe achondroplasia with developmental delay and acanthosis nigricans (SADDAN): phenotypic analysis of a new skeletal dysplasia caused by a Lys650Met mutation in fibroblast growth factor receptor 3G A Bellus, M J Bamshad, K A Przylepa, et al.Genomics|October 27, 1997
Novel genes mapping to the critical region of the 5q- syndromeJ Boultwood, C Fidler, P Soularue, et al.Cytogenetic and Genome Research|February 14, 2003
Physical map of the chromosome 6q22 region containing the oculodentodigital dysplasia locus: analysis of thirteen candidate genes and identification of novel ESTs and DNA polymorphismsS A Boyadjiev, A B Chowdry, R E Shapiro, et al.Gastroenterology|October 31, 1998
American families with Crohn's disease have strong evidence for linkage to chromosome 16 but not chromosome 12S R Brant, Y Fu, C T Fields, et al.Pageof 11