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American Journal of Medical Genetics. Part A|November 24, 2011
Familial Poland anomaly revisitedAnwar Baban, Michele Torre, Sara Costanzo, et al.
American Journal of Medical Genetics. Part A|February 9, 2012
Unusual ribbon-like periventricular heterotopia with congenital cataracts in a Japanese girlRie Tsuburaya, Mitsugu Uematsu, Atsuo Kikuchi, et al.
American Journal of Medical Genetics. Part A|February 9, 2012
Call for change in prenatal counseling for Down syndromeLinda L McCabe, Edward R B McCabe
American Journal of Medical Genetics. Part A|February 9, 2012
Third case of 8q23.3-q24.13 deletion in a patient with Langer-Giedion syndrome phenotype without TRPS1 gene deletionNina Pereza, Srećko Severinski, Saša Ostojić, et al.
American Journal of Medical Genetics. Part A|February 7, 2012
Adams-Oliver syndrome and portal hypertension: fortuitous association or common mechanism?Gisela Silva, Alexandre Braga, Banquart Leitão, et al.
American Journal of Medical Genetics. Part A|February 7, 2012
WDR62 missense mutation in a consanguineous family with primary microcephalyCarlos A Bacino, Luis A Arriola, Joanna Wiszniewska, et al.
American Journal of Medical Genetics. Part A|January 17, 2012
Novel CLDN14 mutations in Pakistani families with autosomal recessive non-syndromic hearing lossKwanghyuk Lee, Muhammad Ansar, Paula B Andrade, et al.
American Journal of Medical Genetics. Part A|January 17, 2012
Segmental maternal uniparental disomy 7q associated with DLK1/GTL2 (14q32) hypomethylationMatthias Begemann, Sabrina Spengler, Ulrike Kordass, et al.
American Journal of Medical Genetics. Part A|January 17, 2012
Nationwide survey of nevoid basal cell carcinoma syndrome in Japan revealing the low frequency of basal cell carcinomaMamiko Endo, Katsunori Fujii, Katsuo Sugita, et al.
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