Binder phenotype: clinical and etiological heterogeneity of the so-called Binder maxillonasal dysplasia in prenatally diagnosed cases, and review of the literature-Reference-Cited by-同舟云学术

Binder phenotype: clinical and etiological heterogeneity of the so-called Binder maxillonasal dysplasia in prenatally diagnosed cases, and review of the literature

Published:2009-02 Issue:2 Volume:29 Page:140-150
ISSN:0197-3851
Container-title:Prenatal Diagnosis
language:en
Short-container-title:Prenat. Diagn.

Author:

Levaillant J. M.,Moeglin D.,Zouiten K.,Bucourt M.,Burglen L.,Soupre V.,Baumann C.,Jaquemont M. L.,Touraine R.,Picard A.,Vuillard E.,Belarbi N.,Oury J. F.,Verloes A.,Vazquez M. P.,Labrune P.,Delezoide A. L.,Gérard-Blanluet M.

Publisher

Wiley

Subject

Genetics (clinical),Obstetrics and Gynecology

Reference42 articles.

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2. Chondrodysplasis punctata: is maternal warfarin therapy a factor?;Becker;Am J Dis Child,1975

3. Dysostosis maxillo-nasalis, ein arhinencephaler Missbildungskomplex;Binder;Deutsch Zahnaerztl DZZ,1962

4. X-linked recessive chondrodysplasia punctata: spectrum of arylsulfatase E gene mutations and expanded clinical variability;Brunetti-Pierri;Am J Med Genet A,2003

5. Molecular structure, chromosome assignment, and promoter organization of the human matrix Gla protein gene;Cancela;J Biol Chem,1990

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