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American Journal of Medical Genetics|October 6, 1999
Aortic root dilation in apparent Lujan-Fryns syndromeL M Wittine, K D Josephson, M S WilliamsAmerican Journal of Medical Genetics|January 24, 1998
Unusual autosomal recessive lymphatic anomalies in two unrelated Amish familiesM S Williams, K D JosephsonClinical Dysmorphology|July 1, 1993
Marden-Walker syndrome: a case report and a critical review of the literatureM S Williams, K D Josephson, D S WargowskiClinical Dysmorphology|July 1, 1995
Patterson-Lowry rhizomelic dysplasia: a possible second exampleM S Williams, K D Josephson, R M PauliGenetics in Medicine : Official Journal of the American College of Medical Genetics|August 2, 2001
Suspected gonadal mosaicism for isochromosomes 18p and 18q unsubstantiated by fluorescence in situ hybridization analysis of spermM S Williams, K D Josephson, N Gursoy, et al.American Journal of Medical Genetics|January 31, 1997
Smith-Lemli-Opitz syndrome: thirty-year follow-up of "S" of "RSH" syndromeR M Pauli, M S Williams, K D Josephson, et al.American Journal of Medical Genetics|June 8, 2001
Klippel-Feil anomaly with Sprengel anomaly, omovertebral bone, thumb abnormalities, and flexion-crease changes: novel association or syndrome?A R Larson, K D Josephson, R M Pauli, et al.American Journal of Medical Genetics|December 31, 1997
Autosomal dominant hypohidrotic ectodermal dysplasia in a large familyA L Aswegan, K D Josephson, R Mowbray, et al.Public Health Genomics|April 11, 2012
The public health genomics translation gap: what we don't have and why it mattersM S WilliamsVeterinary Microbiology|November 1, 1993
Single-radial-immunodiffusion as an in vitro potency assay for human inactivated viral vaccinesM S WilliamsPageof 7