A cytogenetic study in 120 Turkish children with intellectual disability and characteristics of fragile X syndrome

We review the evidence for the frequency of the fragile X syndrome (FXS), other X-linked abnormalities, and other chromosomal disabilities of Turkish pediatric psychiatry outpatients with intellectual disability. Reported clinical features and genetic findings were used in cytogenetic screenings to...

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Veröffentlicht in:	Yonsei medical journal 2003-08, Vol.44 (4), p.583-592
Hauptverfasser:	Demirhan, Osman, Taştemir, Deniz, Diler, Rasim Somer, Firat, Sunay, Avci, Ayse
Format:	Artikel
Sprache:	eng
Schlagworte:	Case-Control Studies Child Child, Preschool Cytogenetic Analysis Female Fragile X Syndrome - genetics Humans Infant Intellectual Disability - genetics Male Turkey
Online-Zugang:	Volltext
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