The Tyr978X BRCA1 mutation: occurrence in non-Jewish Iranians and haplotype in French-Canadian and non-Ashkenazi Jews
Lluís Quintana‐Murci(Centre National de la Recherche Scientifique), Eitan Friedman(Institute of Genetics), Ken McElreavey(Inserm), Ruth Gershoni Baruch(Rambam Health Care Campus), Hélène Quach(Centre National de la Recherche Scientifique), Ronit Shiri‐Sverdlov(Maastricht University), Steven A. Narod(Women's College Hospital), S.Hamid Sayar, Tangiz Bakhan(Sheba Medical Center), Inbar Gal(Sheba Medical Center), Efrat Dagan(University of Haifa)
Cited by 9
Related Papers
Average Risks of Breast and Ovarian Cancer Associated with BRCA1 or BRCA2 Mutations Detected in Case Series Unselected for Family History: A Combined Analysis of 22 Studies
|The American Journal of Human Genetics|2003|3.7k
Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism
|Nature Genetics|2003|1.8k
TLR3 Deficiency in Patients with Herpes Simplex Encephalitis
|Science|2007|1.1k
Breast Cancer Mortality After a Diagnosis of Ductal Carcinoma In Situ
|JAMA Oncology|2015|618