Reversible kallmann syndrome, delayed puberty, and isolated anosmia occurring in a single family with a mutation in the fibroblast growth factor receptor 1 gene.

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Bibliographic Details
Title: Reversible kallmann syndrome, delayed puberty, and isolated anosmia occurring in a single family with a mutation in the fibroblast growth factor receptor 1 gene.
Authors: Pitteloud N; Reproductive Endocrine Unit and National Center for Infertility Research, Bartlett Hall Extension 5, Massachusetts General Hospital, Boston, Massachusetts 02114, USA. npitteloud@partners.org, Acierno JS Jr, Meysing AU, Dwyer AA, Hayes FJ, Crowley WF Jr
Source: The Journal of clinical endocrinology and metabolism [J Clin Endocrinol Metab] 2005 Mar; Vol. 90 (3), pp. 1317-22. Date of Electronic Publication: 2004 Dec 21.
Publication Type: Journal Article; Research Support, U.S. Gov't, P.H.S.
Journal Info: Publisher: Oxford University Press Country of Publication: United States NLM ID: 0375362 Publication Model: Print-Electronic Cited Medium: Print ISSN: 0021-972X (Print) Linking ISSN: 0021972X NLM ISO Abbreviation: J Clin Endocrinol Metab Subsets: MEDLINE
Database: MEDLINE Ultimate
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