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American Journal of Human Genetics|May 1, 1993
Molecular analysis of the 18q- syndrome--and correlation with phenotypeA D Kline, M E White, R Wapner, et al.American Journal of Medical Genetics|September 1, 1994
Aarskog-Scott syndrome: confirmation of linkage to the pericentromeric region of the X chromosomeR E Stevenson, M May, J F Arena, et al.American Journal of Medical Genetics|February 15, 1993
Further delineation of spondylo-meta-epiphyseal dysplasia, short limb-abnormal calcification type, with emphasis on diagnostic featuresL O Langer, B J Wolfson, C I Scott, et al.Human Genetics|February 1, 1995
Genetic homogeneity of cartilage-hair hypoplasiaT Sulisalo, I van der Burgt, D L Rimoin, et al.The Journal of Pediatrics|March 1, 1984
Apnea and sudden unexpected death in infants with achondroplasiaR M Pauli, C I Scott, E R Wassman, et al.Clinical Genetics|September 9, 2015
IRF6 mutation screening in non-syndromic orofacial clefting: analysis of 1521 familiesE J Leslie, D C Koboldt, C J Kang, et al.American Journal of Medical Genetics|June 13, 1997
Lateral meningocele syndrome: three new patients and review of the literatureK W Gripp, C I Scott, H E Hughes, et al.Journal of Dental Research|February 29, 2012
Association of AXIN2 with non-syndromic oral clefts in multiple populationsA Letra, B Bjork, M E Cooper, et al.Pageof 14