Identification of a novel EXT1 mutation in patients with hereditary multiple exostosis by exome sequencing

By  

Oncology Reports, Vol. 33, Iss. 2, 2015-02 ,pp. : 547-552

Spandidos Publications

Access to resources Recommend Favorite

Novel EXT1 mutation identified in a pedigree with hereditary multiple exostoses

By                  

Oncology Reports, Vol. 31, Iss. 2, 2014-01 ,pp. : 713-718

Spandidos Publications

Access to resources Recommend Favorite

Frameshift mutation in the PTCH2 gene can cause nevoid basal cell carcinoma syndrome

By Fujii Katsunori   Ohashi Hirofumi   Suzuki Maiko   Hatsuse Hiromi   Shiohama Tadashi   Uchikawa Hideki   Miyashita Toshiyuki  

Familial Cancer, Vol. 12, Iss. 4, 2013-12 ,pp. : 611-614

Springer Publishing Company

Access to resources Recommend Favorite

Identification of a new complex deleterious mutation in exon 18 of the BRCA2 gene in a hereditary male/female breast cancer family

By Diez Orland  

Breast Cancer Research and Treatment, Vol. 123, Iss. 2, 2010-09 ,pp. : 587-590

Springer Publishing Company

Access to resources Recommend Favorite

A novel mutation of the Succinate Dehydrogenase B Gene in a Korean Family with Pheochromocytoma

By Lee Sang   Kim Eun   Lee Yu   Lee Woochang   Min Won   Lee Young-Joo   Huh Joo   Lee Woo  

Familial Cancer, Vol. 9, Iss. 4, 2010-12 ,pp. : 643-646

Springer Publishing Company

Access to resources Recommend Favorite