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American Journal of Medical Genetics|July 16, 1999
Identification of nine novel mutations in cartilage oligomeric matrix protein in patients with pseudoachondroplasia and multiple epiphyseal dysplasiaM Deere, T Sanford, C A Francomano, et al.American Journal of Medical Genetics|June 13, 1997
Extended survival in a new case of ter Haar syndrome: further delineation of the syndromeR Wallerstein, C I Scott, L NicholsonAmerican Journal of Human Genetics|June 1, 1993
Nonsyndromic cleft lip and palate: no evidence of linkage to HLA or factor 13AJ T Hecht, Y Wang, B Connor, et al.American Journal of Medical Genetics|November 1, 1991
Cognitive and motor skills in achondroplastic infants: neurologic and respiratory correlatesJ T Hecht, N M Thompson, T Weir, et al.Journal of Dental Research|May 7, 2014
Functional Significance of MMP3 and TIMP2 Polymorphisms in Cleft Lip/PalateA Letra, M Zhao, R M Silva, et al.Prenatal Diagnosis|August 1, 1997
Recurrent severe infantile cortical hyperostosis (Caffey disease) in siblingsB M Drinkwater, J P Crino, J Garcia, et al.Clinical Orthopaedics and Related Research|January 11, 2000
Involvement of the humerus in two generations with spondyloepiphyseal dysplasiaU Givon, S J Kumar, C I ScottClinical Dysmorphology|October 1, 1996
Bilateral duplication of the primary ulnar ossification center in Ellis-van Creveld syndromeK W Gripp, C I Scott, L NicholsonAmerican Journal of Medical Genetics|February 2, 1996
Apparently new syndrome of congenital cataracts, sensorineural deafness, Down syndrome-like facial appearance, short stature, and mental retardationK W Gripp, L Nicholson, C I ScottClinical Orthopaedics and Related Research|June 1, 1986
Pelvic dysplasia associated with arthrogrypotic changes in the lower extremities. A new syndromeS Ray, P D Peterson, C I ScottPageof 14