Showing results (11-20 of 30) with videos related to
Sort By:
Pageof 3
Clinical Genetics|January 1, 1983
High resolution chromosome banding in the Rubinstein-Taybi syndromeE A Wulfsberg, I J Klisak, R S SparkesJAMA|January 19, 1994
Alpha 1-antitrypsin deficiency. Impact of genetic discovery on medicine and societyE A Wulfsberg, D E Hoffmann, M M CohenAmerican Journal of Medical Genetics|August 5, 2000
Third Prader-Willi syndrome phenotype due to maternal uniparental disomy 15 with mosaic trisomy 15E Olander, J Stamberg, L Steinberg, et al.American Journal of Medical Genetics|April 1, 1992
Vertebral hypersegmentation in a case of the VATER associationE A Wulfsberg, T L Phillips-Dawkins, R L ThomasJournal of Medical Genetics|April 1, 1984
Trisomy 18 phenotype in a patient with an isopseudodicentric 18 chromosomeE A Wulfsberg, R S Sparkes, I J Klisak, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1994
Phenotypic variability of del(2) (q22-q23): report of a case with a review of the literatureI W Lurie, K R Supovitz, L S Rosenblum-Vos, et al.American Journal of Medical Genetics|December 1, 1982
A 15 leads to 1 translocation in a patient mosaic for presence or absence of an isodic(15p)(q11)E A Wulfsberg, R S Sparkes, I J Klisak, et al.American Journal of Medical Genetics|June 28, 1996
Confirmation of the Catania brachydactylous type of acrofacial dysostosis: report of a second familyE A Wulfsberg, A B Campbell, I W Lurie, et al.American Journal of Medical Genetics|November 1, 1990
Acrofacial dysostosis with ambiguous genitaliaE A Wulfsberg, J Curtis, T E Wiswell, et al.American Journal of Medical Genetics|March 1, 1989
Chromosome 10qter deletion syndrome: a review and report of three new casesE A Wulfsberg, R P Weaver, C M Cunniff, et al.Pageof 3