Interstitial deletion of the short arm of chromosome 10 del(10)(p11.2p12.32) in a patient with congenital heart disease, minor dysmorphism, and mental retardation

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Bibliographische Detailangaben
Veröffentlicht in:	American journal of medical genetics. Part A 2008-12, Vol.146A (24), p.3223-3226
Hauptverfasser:	Behjati, Farkhondeh, Shafeghati, Yousef, Kahrizi, Kimia, Firouzabadi, Saghar Ghasemi, Najmabadi, Hossein, Dixon, Neil, Davies, Angela F.
Format:	Artikel
Sprache:	eng
Schlagworte:	Abnormalities, Multiple - genetics Adult Adult and adolescent clinical studies Biological and medical sciences Child Chromosome Deletion Chromosome Mapping Chromosomes, Human, Pair 10 - genetics Female Heart Defects, Congenital - complications Heart Defects, Congenital - genetics Humans Intellectual deficiency Intellectual Disability - complications Intellectual Disability - genetics Karyotyping Male Medical genetics Medical sciences Psychology. Psychoanalysis. Psychiatry Psychopathology. Psychiatry
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