- Titre
- Inguinal Hernia in a Phenotypic Female Infant May Reveal a 46XY Sex Reversal, Supported by the Identification of a Novel SF1 Gene Mutation
- Créateurs - sans rôle
- Sunik K. Sinha - SUNY Downstate Childrens Hosp, Maimonides Med Ctr, Dept Paediat Endocrinol, Div Pediat Endocrinol, Brooklyn, NY USAPascal Philibert - CHU Montpellier, Hop Lapeyronie, Serv Hormonol, Montpellier, FranceCharles Sultan - CHU Montpellier, Hop Lapeyronie, Serv Hormonol, Montpellier, FranceSvetlana Ten - SUNY Downstate Childrens Hosp, Maimonides Med Ctr, Dept Paediat Endocrinol, Div Pediat Endocrinol, Brooklyn, NY USA
- Contributeurs - sans rôle
- M I NewJ L Simpson
- Détails de publication
- HORMONAL AND GENETIC BASIS OF SEXUAL DIFFERENTIATION DISORDERS AND HOT TOPICS IN ENDOCRINOLOGY, Vol.707, pp.149-150
- Publications en série
- Advances in Experimental Medicine and Biology
- Éditeur
- Springer Nature
- Nombre de pages
- 2
- Identifiants
- 99139668309311
- Unité académique
- Institut de Génétique Humaine - IGH
- Langue
- English
- Type de ressource
- Journal article
Article de revue
Inguinal Hernia in a Phenotypic Female Infant May Reveal a 46XY Sex Reversal, Supported by the Identification of a Novel SF1 Gene Mutation
HORMONAL AND GENETIC BASIS OF SEXUAL DIFFERENTIATION DISORDERS AND HOT TOPICS IN ENDOCRINOLOGY, Vol.707, pp.149-150
Advances in Experimental Medicine and Biology
01/01/2011
PMID: 21691975
Indicateurs
1 Consultations de la notice