Genetic testing for RAD51C mutations: in the clinic and community

By  

CLINICAL GENETICS, Vol. 9-9163, Iss. 4, 2015-10 ,pp. : 303-312

John Wiley & Sons Inc

Access to resources Recommend Favorite

New Characteristics of Drosophila Mutation RAD(2)201^Gl: Epigenetic Transmission of a Repair Defect via Meiosis and Association with the Rad51C gene

By Khromykh Yu. M.   Varentsova E. R.   Sarantseva S. V.   Kotlovanova L. V.  

Doklady Biological Sciences, Vol. 395, Iss. 1-6, 2004-03 ,pp. : 163-165

MAIK Nauka/Interperiodica

Access to resources Recommend Favorite

Thiopurine‐induced mitotic catastrophe in Rad51d‐deficient mammalian cells

By  

ENVIRONMENTAL AND MOLECULAR MUTAGENESIS (ELECTRONIC), Vol. 59, Iss. 1, 2018-01 ,pp. : 38-48

John Wiley & Sons Inc

Access to resources Recommend Favorite

Genetic testing for sporadic hearing loss using targeted massively parallel sequencing identifies 10 novel mutations

By  

CLINICAL GENETICS, Vol. 87, Iss. 6, 2015-06 ,pp. : 588-593

John Wiley & Sons Inc

Access to resources Recommend Favorite

Development of Genetic Testing for Fragile X Syndrome and Associated Disorders, and Estimates of the Prevalence of FMR1 Expansion Mutations

By Macpherson James N.   Murray Anna  

Genes, Vol. 7, Iss. 12, 2016-11 ,pp. : 110-110

MDPI

Access to resources Recommend Favorite