Literature DB >> 4767905

Median facial cleft syndrome in half-sisters. Dilemmas in genetic counseling.

J Warkany, M K Bofinger, C Benton.   

Abstract

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Year:  1973        PMID： 4767905     DOI： 10.1002/tera.1420080307

Source DB:  PubMed          Journal:  Teratology        ISSN： 0040-3709


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  3 in total

1.  Misexpression of Six2 is associated with heritable frontonasal dysplasia and renal hypoplasia in 3H1 Br mice.

Authors:  Ben Fogelgren; Mari C Kuroyama; Brandeis McBratney-Owen; Allyson A Spence; Laura E Malahn; Mireille K Anawati; Chantelle Cabatbat; Vernadeth B Alarcon; Yusuke Marikawa; Scott Lozanoff
Journal:  Dev Dyn       Date:  2008-07       Impact factor: 3.780

2.  Median cleft face syndrome in association with hydrocephalus, agenesis of the corpus callosum, holoprosencephaly and choanal atresia.

Authors:  T Bömelburg; W Lenz; T Eusterbrock
Journal:  Eur J Pediatr       Date:  1987-05       Impact factor: 3.183

3.  Acromelic frontonasal dysostosis and ZSWIM6 mutation: phenotypic spectrum and mosaicism.

Authors:  S R F Twigg; L B Ousager; K A Miller; Y Zhou; S C Elalaoui; A Sefiani; G S Bak; H Hove; L K Hansen; C R Fagerberg; M Tajir; A O M Wilkie
Journal:  Clin Genet       Date:  2016-02-03       Impact factor: 4.438
  3 in total

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