Human Genome Epidemiology Literature Finder
Records 1 - 2 (of 2 Records)
|Query Trace: 46, XY Disorders of Sex Development and HSD17B3[original query]|
| 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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