Presenting phenotype in 100 children with the 22q11 deletion syndrome-Reference-Cited by-同舟云学术

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Presenting phenotype in 100 children with the 22q11 deletion syndrome

Published:2004-11-23 Issue:3 Volume:164 Page:146-153
ISSN:0340-6199
Container-title:European Journal of Pediatrics
language:en
Short-container-title:Eur J Pediatr

Author:

�skarsd�ttir S�lveig,Persson Christina,Eriksson Bengt O.,Fasth Anders

Publisher

Springer Science and Business Media LLC

Subject

Pediatrics, Perinatology, and Child Health

Link

http://link.springer.com/content/pdf/10.1007/s00431-004-1577-8.pdf

Reference18 articles.

1. Adachi M, Tachibana K, Maasuno M, Makita Y, Maesaka H, Okada T, Hizukuri K, Imaizumi K, Kuroki Y, Kurahasi H, Suwa S (1998) Clinical characteristics of children with hypoparathyroidism due to 22q11.2 microdeletion. Eur J Pediatr 157: 34?38

2. Devriendt K, Fryns JP, Mortier G (1998) The annual incidence of DiGeorge/velocardiofacial syndrome (letter). J Med Genet 35: 789

3. Ghariani S, Dahan K, Saint-Martin C, Kadhim H, Morsomme F, Moniotte S, Verellen-Dumoulin GS (2002) Polymicrogyria in chromosome 22q11 deletion syndrome. Eur J Paediatr Neurol 6: 73?77

4. Johannesson T, Holmqvist D, Martinsson T, Wahlström J (1991) An improved technique for chromosome preparations from human lymphocytes. Hereditas 115: 295?297

5. Kapur P, Caty MG (1998) Pediatric hernias and hydroceles. Pediatr Clin North Am 45: 773?789

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