Genetic evaluation based on family history and Her2 status correctly identifies TP53 mutations in very early onset breast cancer cases

By  

CLINICAL GENETICS, Vol. 87, Iss. 4, 2015-04 ,pp. : 383-387

John Wiley & Sons Inc

Access to resources Recommend Favorite

The Consequence of Oncomorphic TP53 Mutations in Ovarian Cancer

By Brachova Pavla   Thiel Kristina W.   Leslie Kimberly K.  

International Journal of Molecular Sciences, Vol. 14, Iss. 9, 2013-09 ,pp. : 19257-19275

MDPI

Access to resources Recommend Favorite

Nonsyndromic Early‐Onset Cone‐Rod Dystrophy and Limb‐Girdle Muscular Dystrophy in a Consanguineous Israeli Family are Caused by Two Independent yet Linked Mutations in ALMS1 and DYSF

By  

HUMAN MUTATION, Vol. 36, Iss. 9, 2015-09 ,pp. : 836-841

John Wiley & Sons Inc

Access to resources Recommend Favorite

Novel biallelic SZT2 mutations in 3 cases of early‐onset epileptic encephalopathy

By  

CLINICAL GENETICS, Vol. 93, Iss. 2, 2018-02 ,pp. : 266-274

John Wiley & Sons Inc

Access to resources Recommend Favorite

A Next-Generation Sequencing Approach to Identify Gene Mutations in Early- and Late-Onset Hypertrophic Cardiomyopathy Patients of an Italian Cohort

By Rubattu Speranza   Bozzao Cristina   Pennacchini Ermelinda   Pagannone Erika   Musumeci Beatrice Maria   Piane Maria   Germani Aldo   Savio Camilla   Francia Pietro   Volpe Massimo   Autore Camillo   Chessa Luciana  

International Journal of Molecular Sciences, Vol. 17, Iss. 8, 2016-07 ,pp. : 1239-1239

MDPI

Access to resources Recommend Favorite