WAGR syndrome with deletion of chromosome 11p11.2-13

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Veröffentlicht in:	Journal of AAPOS 2004-08, Vol.8 (4), p.396-397
Hauptverfasser:	Pinna, Antonio, Carta, Adolfo, Mannazzu, Maria Chiara, Dore, Stefano, Balata, Antonio, Carta, Francesco
Format:	Artikel
Sprache:	eng
Schlagworte:	Aniridia - diagnosis Cataract - congenital Chromosome Deletion Chromosomes, Human, Pair 11 - genetics Humans Infant, Newborn Male WAGR Syndrome - diagnosis WAGR Syndrome - genetics
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doi_str_mv	10.1016/j.jaapos.2004.05.008
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language	eng
recordid	cdi_proquest_miscellaneous_66791636
source	MEDLINE; ScienceDirect Journals (5 years ago - present)
subjects	Aniridia - diagnosis Cataract - congenital Chromosome Deletion Chromosomes, Human, Pair 11 - genetics Humans Infant, Newborn Male WAGR Syndrome - diagnosis WAGR Syndrome - genetics
title	WAGR syndrome with deletion of chromosome 11p11.2-13
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