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Greater prevalence of PROKR2 mutations in Kallmann syndrome patients from the Maghreb than in European patients.
Sarfati, Julie; Fouveaut, Corinne; Leroy, Chrystel; Jeanpierre, Marc; Hardelin, Jean-Pierre; Dodé, Catherine.
Affiliation
  • Sarfati J; Département de Génétique et Développement, Institut Cochin, Inserm U1016, Université Paris-Descartes, Paris, France.
Eur J Endocrinol ; 169(6): 805-9, 2013 Dec.
Article in En | MEDLINE | ID: mdl-24031091
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Kallmann Syndrome / Receptors, Peptide / Arabs / Receptors, G-Protein-Coupled / White People / Mutation Type of study: Prevalence_studies / Prognostic_studies / Risk_factors_studies Limits: Adult / Aged / Female / Humans / Male / Middle aged Country/Region as subject: Africa / Europa Language: En Journal: Eur J Endocrinol Year: 2013 Document type: Article
Fulltext
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PubMed Links
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Kallmann Syndrome / Receptors, Peptide / Arabs / Receptors, G-Protein-Coupled / White People / Mutation Type of study: Prevalence_studies / Prognostic_studies / Risk_factors_studies Limits: Adult / Aged / Female / Humans / Male / Middle aged Country/Region as subject: Africa / Europa Language: En Journal: Eur J Endocrinol Year: 2013 Document type: Article