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American Journal of Medical Genetics. Part A|October 3, 2018
Multicenter study of mortality in achondroplasiaS Shahrukh Hashmi, Candace Gamble, Julie Hoover-Fong, et al.
American Journal of Human Genetics|October 1, 1992
SSCP and segregation analysis of the human type X collagen gene (COL10A1) in heritable forms of chondrodysplasiaW A Sweetman, B Rash, B Sykes, et al.
American Journal of Medical Genetics. Part A|January 17, 2012
Dominant and recessive forms of fibrochondrogenesis resulting from mutations at a second locus, COL11A2Stuart W Tompson, Eissa Ali Faqeih, Leena Ala-Kokko, et al.
American Journal of Medical Genetics. Part A|August 14, 2008
The population-based prevalence of achondroplasia and thanatophoric dysplasia in selected regions of the USD K Waller, A Correa, Tuan M Vo, et al.
Nature Genetics|July 1, 1995
Mutations in exon 17B of cartilage oligomeric matrix protein (COMP) cause pseudoachondroplasiaJ T Hecht, L D Nelson, E Crowder, et al.
American Journal of Medical Genetics|February 1, 1985
Computerized tomography of the foramen magnum: achondroplastic values compared to normal standardsJ T Hecht, F W Nelson, I J Butler, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|February 6, 2010
Investigator-initiated trials of targeted oncology agents: why independent research is at risk?L Bergmann, B Berns, A G Dalgleish, et al.
Frontiers in Cell and Developmental Biology|February 28, 2022
Genome-wide Interaction Study Implicates <i>VGLL2</i> and Alcohol Exposure and <i>PRL</i> and Smoking in Orofacial Cleft RiskJenna C Carlson, John R Shaffer, Fred Deleyiannis, et al.
Journal of Medical Genetics|March 27, 2014
Genome-wide association study identifies new disease loci for isolated clubfootTian-Xiao Zhang, Gabe Haller, Peng Lin, et al.
American Journal of Medical Genetics. Part A|June 9, 2012
Studies of TBX4 and chromosome 17q23.1q23.2: an uncommon cause of nonsyndromic clubfootW Lu, C A Bacino, B S Richards, et al.
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