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Compound heterozygous mutations in the luteinizing hormone receptor signal peptide causing 46,XY disorder of sex development. [electronic resource] by
- Potorac, Iulia
- Trehan, Ashutosh
- Szymańska, Kamila
- Fudvoye, Julie
- Thiry, Albert
- Huhtaniemi, Ilpo
- Daly, Adrian F
- Beckers, Albert
- Parent, Anne-Simone
- Rivero-Müller, Adolfo
Producer: 20200206
In:
European journal of endocrinology vol. 181
Availability: No items available.
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Recurrent Intragenic Duplication within the NR5A1 Gene and Severe Proximal Hypospadias. [electronic resource] by
- Peycelon, Matthieu
- Mansour-Hendili, Lamisse
- Hyon, Capucine
- Collot, Nathalie
- Houang, Muriel
- Legendre, Marie
- Chabaud, Maud
- Bouvier, Marie-Dominique
- Audry, Georges
- Amselem, Serge
- Siffroi, Jean-Pierre
Producer: 20181022
In:
Sexual development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation vol. 11
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