Literature DB >> 12116215

Craniofrontonasal syndrome and diaphragmatic hernia.

Julie McGaughran, Martin Rees, Malcom Battin.   

Abstract

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Year:  2002        PMID： 12116215     DOI： 10.1002/ajmg.10176

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN： 0148-7299


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  3 in total

Review 1.  Overview of epidemiology, genetics, birth defects, and chromosome abnormalities associated with CDH.

Authors:  Barbara R Pober
Journal:  Am J Med Genet C Semin Med Genet       Date:  2007-05-15       Impact factor: 3.908

2.  Matthew-Wood syndrome is caused by truncating mutations in the retinol-binding protein receptor gene STRA6.

Authors:  Christelle Golzio; Jelena Martinovic-Bouriel; Sophie Thomas; Soumaya Mougou-Zrelli; Bettina Grattagliano-Bessieres; Maryse Bonniere; Sophie Delahaye; Arnold Munnich; Ferechte Encha-Razavi; Stanislas Lyonnet; Michel Vekemans; Tania Attie-Bitach; Heather C Etchevers
Journal:  Am J Hum Genet       Date:  2007-04-11       Impact factor: 11.025

3.  Case Report and Review of the Literature: Congenital Diaphragmatic Hernia and Craniosynostosis, a Coincidence or Common Cause?

Authors:  Linda Gaillard; Anne Goverde; Quincy C C van den Bosch; Fernanda S Jehee; Erwin Brosens; Danielle Veenma; Frank Magielsen; Annelies de Klein; Irene M J Mathijssen; Marieke F van Dooren
Journal:  Front Pediatr       Date:  2021-11-26       Impact factor: 3.418
  3 in total

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