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

Please use this identifier to cite or link to this item: https://olympias.lib.uoi.gr/jspui/handle/123456789/20688

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DC Field	Value	Language
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.type	journalArticle	-
heal.type.en	Journal article	en
heal.type.el	Άρθρο Περιοδικού	el
heal.identifier.secondary	http://www.ncbi.nlm.nih.gov/pubmed/11565549	-
heal.language	en	-
heal.access	campus	-
heal.recordProvider	Πανεπιστήμιο Ιωαννίνων. Σχολή Επιστημών Υγείας. Τμήμα Ιατρικής	el
heal.publicationDate	2001	-
heal.journalName	J Med Genet	en
heal.journalType	peer-reviewed	-
heal.fullTextAvailability	TRUE	-
Appears in Collections:	Άρθρα σε επιστημονικά περιοδικά ( Ανοικτά) - ΙΑΤ

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