Related content

Early-onset severe hereditary sensory and autonomic neuropathy type 1 with S331F SPTLC1 mutation

By            

Molecular Medicine Reports, Vol. 9, Iss. 2, 2014-01 ,pp. : 481-486

Spandidos Publications

Access to resources Recommend Favorite

Two families with Leber's hereditary optic neuropathy carrying G11778A and T14502C mutations with haplogroup H2a2a1 in mitochondrial DNA

By              

Molecular Medicine Reports, Vol. 12, Iss. 2, 2015-01 ,pp. : 3067-3072

Spandidos Publications

Access to resources Recommend Favorite

Novel germline mutations in BRCA2 gene among 96 hereditary breast and breast–ovarian cancer families from Kerala, South India

By Syamala Vani   Sreeja Leelakumari   Syamala Volga   Vinodkumar B.   Raveendran Praveenkumar   Sreedharan Hariharan   Kuttappan Ratheesan   Balakrishnan Lekshmi   Ankathil Ravindran  

Journal of Cancer Research and Clinical Oncology, Vol. 133, Iss. 11, 2007-11 ,pp. : 867-874

Springer Publishing Company

Access to resources Recommend Favorite

Germline Mutations of the hMLH1 and hMSH2 Mismatch Repair Genes in Belgian Hereditary Nonpolyposis Colon Cancer (HNPCC) Patients

By Spaepen M.   Vankeirsbilck B.   Opstal S.   Tejpar S.   Cutsem E.   Geboes K.   Legius E.   Matthijs G.  

Familial Cancer, Vol. 5, Iss. 2, 2006-06 ,pp. : 179-189

Springer Publishing Company

Access to resources Recommend Favorite

Prevalence of BRCA1 and BRCA2 mutations in non-familial breast cancer patients with high risks in Korea: The Korean Hereditary Breast Cancer (KOHBRA) Study

By Son Byung  

Breast Cancer Research and Treatment, Vol. 133, Iss. 3, 2012-06 ,pp. : 1143-1152

Springer Publishing Company

Access to resources Recommend Favorite