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A novel deletion in the GH1 gene including the IVS3 branch site responsible for autosomal dominant isolated growth hormone deficiency.
Vivenza, Daniela; Guazzarotti, Laura; Godi, Michela; Frasca, Daniela; di Natale, Berardo; Momigliano-Richiardi, Patricia; Bona, Gianni; Giordano, Mara.
Affiliation
  • Vivenza D; Dipartimento di Scienze Mediche, Via Solaroli 17, 28100 Novara, Italy.
J Clin Endocrinol Metab ; 91(3): 980-6, 2006 Mar.
Article in En | MEDLINE | ID: mdl-16368751
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Collection: 01-internacional Database: MEDLINE Main subject: Sequence Deletion / Human Growth Hormone Type of study: Prognostic_studies Limits: Child, preschool / Female / Humans / Male Language: En Journal: J Clin Endocrinol Metab Year: 2006 Document type: Article Affiliation country: Italy Country of publication: United States
Search on Google
Add to My VHL
Print
XML
PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: Sequence Deletion / Human Growth Hormone Type of study: Prognostic_studies Limits: Child, preschool / Female / Humans / Male Language: En Journal: J Clin Endocrinol Metab Year: 2006 Document type: Article Affiliation country: Italy Country of publication: United States