Human Genome Epidemiology Literature Finder
Records 1 - 2 (of 2 Records) |
Query Trace: 46, XY Disorders of Sex Development and HSD17B3[original query] |
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Screening for mutations in 17ß-hydroxysteroid dehydrogenase and androgen receptor in women presenting with partially virilised 46,XY disorders of sex development. European journal of endocrinology / European Federation of Endocrine Societies 2015 Mar . Phelan Niamh, Williams Emma L, Cardamone Stefanie, Lee Marilyn, Creighton Sarah M, Rumsby Gill, Conway Gerard |
Novel cases of Tunisian patients with mutations in the gene encoding 17ß-hydroxysteroid dehydrogenase type 3 and a founder effect. The Journal of steroid biochemistry and molecular biology 2016 Mar . Ben Rhouma Bochra, Kallabi Fakhri, Mahfoudh Nadia, Ben Mahmoud Afif, Engeli Roger T, Kamoun Hassen, Keskes Leila, Odermatt Alex, Belguith Nei |
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- Page last updated:May 30, 2023
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