Showing results (31-40 of 61) with videos related to

Sort By:
Pageof 7
Journal of Human Genetics|April 24, 2010
DHPLC screening for mutations in progressive familial intrahepatic cholestasis patientsRivka Shapiro, Yair Anikster, Tal Yardeni, et al.
Thyroid : Official Journal of the American Thyroid Association|January 6, 2015
Long-term outcome of loss-of-function mutations in thyrotropin receptor geneYardena Tenenbaum-Rakover, Shlomo Almashanu, Ora Hess, et al.
The Journal of Cell Biology|October 23, 2002
Central role of alpha7 nicotinic receptor in differentiation of the stratified squamous epitheliumJuan Arredondo, Vu Thuong Nguyen, Alexander I Chernyavsky, et al.
European Journal of Haematology|April 3, 2004
Molecular characterization of three novel Fanconi anemia mutations in Israeli ArabsHannah Tamary, Orly Dgany, Helen Toledano, et al.
American Journal of Human Genetics|September 9, 2006
A deleterious mutation in SAMD9 causes normophosphatemic familial tumoral calcinosisOrit Topaz, Margarita Indelman, Ilana Chefetz, et al.
American Journal of Human Genetics|February 9, 2010
Autosomal-recessive hypophosphatemic rickets is associated with an inactivation mutation in the ENPP1 geneVarda Levy-Litan, Eli Hershkovitz, Luba Avizov, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|February 21, 2003
Central role of fibroblast alpha3 nicotinic acetylcholine receptor in mediating cutaneous effects of nicotineJuan Arredondo, Leon L Hall, Assane Ndoye, et al.
Diseases of the Colon and Rectum|August 8, 2018
POLD1 and POLE Gene Mutations in Jewish Cohorts of Early-Onset Colorectal Cancer and of Multiple Colorectal AdenomasGuy Rosner, Nathan Gluck, Shai Carmi, et al.
Pageof 7