Study of smell and reproductive organs in a mouse model for CHARGE syndrome
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics(clinical),Genetics
Link
http://www.nature.com/articles/ejhg2009158.pdf
Reference35 articles.
1. Pagon RA, Graham Jr JM, Zonana J, Yong SL : Coloboma, congenital heart disease, and choanal atresia with multiple anomalies: CHARGE association. J Pediatr 1981; 99: 223–227.
2. Amiel J, Attiee-Bitach T, Marianowski R et al: Temporal bone anomaly proposed as a major criteria for diagnosis of CHARGE syndrome. Am J Med Genet 2001; 99: 124–127.
3. Chalouhi C, Faulcon P, Le Bihan C, Hertz-Pannier L, Bonfils P, Abadie V : Olfactory evaluation in children: application to the CHARGE syndrome. Pediatrics 2005; 116: e81–e88.
4. Pinto G, Abadie V, Mesnage R et al: CHARGE syndrome includes hypogonadotropic hypogonadism and abnormal olfactory bulb development. J Clin Endocrinol Metab 2005; 90: 5621–5626.
5. Sanlaville D, Etchevers HC, Gonzales M et al: Phenotypic spectrum of CHARGE syndrome in fetuses with CHD7 truncating mutations correlates with expression during human development. J Med Genet 2006; 43: 211–217.
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