A MOLECULARLY CHARACTERIZED INTERSTITIAL DELETION ENCOMPASSING THE 11q14.1-q23.3 REGION IN A CASE WITH MULTIPLE CONGENITAL ABNORMALITIES.

Cetin, Z; Altiok-Clark, O; Yakut, S; Guzel-Nur, B; Mihci, E; Berker-Karauzum, S

Cetin, Z; Altiok-Clark, O; Yakut, S; Guzel-Nur, B; Mihci, E; Berker-Karauzum, S.

Genet Couns ; 27(1): 51-66, 2016.

Article in En | MEDLINE | ID: mdl-27192892

Subject(s)

Abnormalities, Multiple/genetics; Chromosome Deletion; Chromosomes, Human, Pair 11/genetics; Intellectual Disability/genetics; Adolescent; Cytogenetic Analysis; Humans; Male

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Collection: 01-internacional Database: MEDLINE Main subject: Abnormalities, Multiple / Chromosomes, Human, Pair 11 / Chromosome Deletion / Intellectual Disability Limits: Adolescent / Humans / Male Language: En Journal: Genet Couns Journal subject: ETICA / GENETICA MEDICA Year: 2016 Type: Article

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