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

CDC 25A gene 263C/T, - 350C /T, and -51C/G polymorphisms in breast carcinoma

By Karagoz Isik  

Tumor Biology, Vol. 31, Iss. 6, 2010-12 ,pp. : 597-604

Springer Publishing Company

Access to resources Recommend Favorite

Effects of the Smad4 C324Y mutation on thyroid cell proliferation

By        

International Journal of Oncology, Vol. 42, Iss. 6, 2013-01 ,pp. : 1890-1896

Spandidos Publications

Access to resources Recommend Favorite

Identification of a novel BRCA1 nucleotide 4803delCC/c.4684delCC mutation and a nucleotide 249T>A/c.130T>A (p.Cys44Ser) mutation in two Greenlandic Inuit families: implications for genetic screening of Greenlandic Inuit families with high risk for breast and/or ovarian cancer

By Hansen Thomas  

Breast Cancer Research and Treatment, Vol. 124, Iss. 1, 2010-11 ,pp. : 259-264

Springer Publishing Company

Access to resources Recommend Favorite

Mutation analysis of two families with inherited congenital cataracts

By Liang Chang   Liang Han   Yang Yu   Ping Liu   Jie Qiao  

Molecular Medicine Reports, Vol. 12, Iss. 3, 2015-09 ,pp. : 3469-3475

Spandidos Publications

Access to resources Recommend Favorite