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The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|August 10, 2016
Hypertelorism and Orofacial Clefting Revisited: An Anthropometric InvestigationSeth M Weinberg, Elizabeth J Leslie, Jacqueline T Hecht, et al.American Journal of Hypertension|May 21, 2014
Essential hypertension vs. secondary hypertension among childrenMonesha Gupta-Malhotra, Ashish Banker, Sanjay Shete, et al.American Journal of Human Genetics|August 1, 1995
Nonsyndromic cleft lip with or without cleft palate: evidence of linkage to BCL3 in 17 multigenerational familiesJ Stein, J B Mulliken, S Stal, et al.Nature Genetics|July 1, 1995
A recurrent mutation in the tyrosine kinase domain of fibroblast growth factor receptor 3 causes hypochondroplasiaG A Bellus, I McIntosh, E A Smith, et al.American Journal of Medical Genetics. Part A|November 26, 2009
Altered transmission of HOX and apoptotic SNPs identify a potential common pathway for clubfootAudrey R Ester, Katelyn S Weymouth, Amber Burt, et al.American Journal of Human Genetics|January 11, 1991
Analysis of the chondroitin sulfate proteoglycan core protein (CSPGCP) gene in achondroplasia and pseudoachondroplasiaJ E Finkelstein, K Doege, Y Yamada, et al.Birth Defects Research|April 7, 2019
Association of IFT88 gene variants with nonsyndromic cleft lip with or without cleft palateAmanda Barba, Christian Urbina, Lorena Maili, et al.American Journal of Human Genetics|November 1, 1994
Evidence, from family studies, for linkage disequilibrium between TGFA and a gene for nonsyndromic cleft lip with or without cleft palateH Feng, R Sassani, S P Bartlett, et al.American Journal of Human Genetics|February 1, 1995
Achondroplasia is defined by recurrent G380R mutations of FGFR3G A Bellus, T W Hefferon, R I Ortiz de Luna, et al.Genomics|June 15, 1996
Localization of the homolog of a mouse craniofacial mutant to human chromosome 18q11 and evaluation of linkage to human CLP and CPOA J Griffith, D L Burgess, D C Kohrman, et al.Pageof 34