Microdeletion 2q23.1 and syndromic findings

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Veröffentlicht in:	Revista de neurologiá 2013-11, Vol.57 (9), p.430
Hauptverfasser:	Pérez-Gay, Laura, Gómez-Lado, Carmen, Eirís-Puñal, Jesús, Dacruz, David, Quintela, Inés, Barros-Angueira, Francisco, Castro-Gago, Manuel
Format:	Artikel
Sprache:	spa
Schlagworte:	Abnormalities, Multiple - genetics Chromosome Deletion Chromosomes, Human, Pair 2 - genetics Developmental Disabilities - genetics Epilepsy - genetics Humans Infant Male Syndrome
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doi_str_mv	10.33588/rn.5709.2013326
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source	MEDLINE; EZB-FREE-00999 freely available EZB journals
subjects	Abnormalities, Multiple - genetics Chromosome Deletion Chromosomes, Human, Pair 2 - genetics Developmental Disabilities - genetics Epilepsy - genetics Humans Infant Male Syndrome
title	Microdeletion 2q23.1 and syndromic findings
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