Bibliographic Details
| Title: |
Mutations in fibroblast growth factor receptor 1 cause Kallmann syndrome with a wide spectrum of reproductive phenotypes. |
| Authors: |
Pitteloud N; Reproductive Endocrine Unit of the Department of Medicine & National Center for Infertility Research, Bartlett Hall Extension 5, Massachusetts General Hospital, 55 Fruit St., Boston, MA 02114, United States. npitteloud@partners.org, Meysing A, Quinton R, Acierno JS Jr, Dwyer AA, Plummer L, Fliers E, Boepple P, Hayes F, Seminara S, Hughes VA, Ma J, Bouloux P, Mohammadi M, Crowley WF Jr |
| Source: |
Molecular and cellular endocrinology [Mol Cell Endocrinol] 2006 Jul 25; Vol. 254-255, pp. 60-9. Date of Electronic Publication: 2006 Jun 09. |
| Publication Type: |
Journal Article; Research Support, N.I.H., Extramural |
| Journal Info: |
Publisher: North Holland Publishing Country of Publication: Ireland NLM ID: 7500844 Publication Model: Print-Electronic Cited Medium: Print ISSN: 0303-7207 (Print) Linking ISSN: 03037207 NLM ISO Abbreviation: Mol Cell Endocrinol Subsets: MEDLINE |
| Database: |
MEDLINE Ultimate |
