Muenke syndrome (FGFR3-related craniosynostosis): expansion of the phenotype and review of the literature.

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Bibliographic Details
Title: Muenke syndrome (FGFR3-related craniosynostosis): expansion of the phenotype and review of the literature.
Authors: Doherty ES; National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, USA., Lacbawan F, Hadley DW, Brewer C, Zalewski C, Kim HJ, Solomon B, Rosenbaum K, Domingo DL, Hart TC, Brooks BP, Immken L, Lowry RB, Kimonis V, Shanske AL, Jehee FS, Bueno MR, Knightly C, McDonald-McGinn D, Zackai EH, Muenke M
Source: American journal of medical genetics. Part A [Am J Med Genet A] 2007 Dec 15; Vol. 143A (24), pp. 3204-15.
Publication Type: Journal Article; Research Support, N.I.H., Intramural
Journal Info: Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 101235741 Publication Model: Print Cited Medium: Internet ISSN: 1552-4833 (Electronic) Linking ISSN: 15524825 NLM ISO Abbreviation: Am J Med Genet A Subsets: MEDLINE
Database: MEDLINE Ultimate
Description
ISSN:1552-4833
DOI:10.1002/ajmg.a.32078