A newborn diagnosed with van Maldergem syndrome-Reference-Cited by-同舟云学术

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A newborn diagnosed with van Maldergem syndrome

Published:2018-04 Issue:2 Volume:27 Page:63-65
ISSN:0962-8827
Container-title:Clinical Dysmorphology
language:en
Short-container-title:

Author:

Ulubas Isik Dilek,Unal Sezin,Erol Sara,Arslan Zehra,Bas Ahmet Y.,Demirel Nihal

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Genetics (clinical),General Medicine,Pathology and Forensic Medicine,Anatomy,Pediatrics, Perinatology and Child Health

Reference8 articles.

1. A second family with blepharo-naso-facial syndrome;Allanson;Clin Dysmorphol,2002

2. Mutations in genes encoding the cadherin receptor-ligand pair DCHS1 and FAT4 disrupt cerebral cortical development;Cappello;Nature Genet,2013

3. Autosomal recessive intestinal lymphangiectasia and lymphedema, with facial anomalies and mental retardation;Hennekam;Am J Med Genet,1989

4. Van Maldergem syndrome: further characterisation and evidence for neuronal migration abnormalities and autosomal recessive inheritance;Mansour;Europ J Hum Genet,2012

5. A further patient with van Maldergem syndrome;Neuhann;Eur J Med Genet,2012

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