Interstitial deletion of chromosome 11 (q22.3-q23.2) in a boy with mild developmental delay

dc.contributor.author	Syrrou, M.	en
dc.contributor.author	Fryns, J. P.	en
dc.date.accessioned	2015-11-24T19:09:19Z
dc.date.available	2015-11-24T19:09:19Z
dc.identifier.issn	1468-6244	-
dc.identifier.uri	https://olympias.lib.uoi.gr/jspui/handle/123456789/20688
dc.rights	Default Licence	-
dc.subject	Child, Preschool	en
dc.subject	Chromosome Banding	en
dc.subject	*Chromosome Deletion	en
dc.subject	Chromosome Fragility/genetics	en
dc.subject	Chromosomes, Human, Pair 11/*genetics	en
dc.subject	Developmental Disabilities/*genetics	en
dc.subject	Female	en
dc.subject	Humans	en
dc.subject	In Situ Hybridization, Fluorescence	en
dc.subject	Infant	en
dc.subject	Karyotyping	en
dc.subject	Male	en
dc.subject	Models, Genetic	en
dc.subject	Phenotype	en
dc.subject	Psychomotor Performance	en
dc.title	Interstitial deletion of chromosome 11 (q22.3-q23.2) in a boy with mild developmental delay	en
heal.access	campus	-
heal.fullTextAvailability	TRUE	-
heal.identifier.secondary	http://www.ncbi.nlm.nih.gov/pubmed/11565549	-
heal.journalName	J Med Genet	en
heal.journalType	peer-reviewed	-
heal.language	en	-
heal.publicationDate	2001	-
heal.recordProvider	Πανεπιστήμιο Ιωαννίνων. Σχολή Επιστημών Υγείας. Τμήμα Ιατρικής	el
heal.type	journalArticle	-
heal.type.el	Άρθρο Περιοδικού	el
heal.type.en	Journal article	en

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