Deletion in chromosome region 22q11 in a child with CHARGE association
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1998.tb02755.x/fullpdf
Reference17 articles.
1. Isolation of a new marker and conserved sequences close to the DiGeorge syndrome marker HP500 (D22S134);Wadey;J Med Genet,1993
2. Coloboma, congenital heart disease, and choanal atresia with multiple anomalies: CHARGE association;Pagon;Pediatrics,1981
3. Familial CHARGE association: affected half siblings through a normal mother;Hall;Am J Hum Genet,1988
4. Dominant CHARGE association;Mitchell;Ophthalmic Paediatr Genet,1985
5. Familial CHARGE syndrome: clinical report with autopsy findings;Metlay;Am J Med Genet,1987
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4. Chromosome 22 microdeletion in children with syndromic congenital heart disease by fluorescent in situ hybridization (FISH);Egyptian Journal of Medical Human Genetics;2012-10
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