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FEBS Letters|March 8, 1993
A human synaptic vesicle monoamine transporter cDNA predicts posttranslational modifications, reveals chromosome 10 gene localization and identifies TaqI RFLPsC K Surratt, A M Persico, X D Yang, et al.Nature Genetics|August 1, 1996
Fibroblast growth factor receptor 2 mutations in Beare-Stevenson cutis gyrata syndromeK A Przylepa, W Paznekas, M Zhang, et al.Neuromuscular Disorders : NMD|September 1, 1994
Development of a microsatellite genetic map spanning 5q31-q33 and subsequent placement of the LGMD1A locus between D5S178 and IL9L H Yamaoka, C A Westbrook, M C Speer, et al.Nature Genetics|January 1, 1997
Mutations in TWIST, a basic helix-loop-helix transcription factor, in Saethre-Chotzen syndromeT D Howard, W A Paznekas, E D Green, et al.Journal of Medical Genetics|January 18, 2006
High throughput SNP and expression analyses of candidate genes for non-syndromic oral cleftsJ W Park, J Cai, I McIntosh, et al.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.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.Pageof 11