Cyclopia, proboscis and alobar holoprosencephaly representative for trisomy 13.

Bozkurt, O; Kanmaz, H G; Sahin, S; Canpolat, F E; Uras, N; Oguz, S S; Dilmen, U

Bozkurt, O; Kanmaz, H G; Sahin, S; Canpolat, F E; Uras, N; Oguz, S S; Dilmen, U.

Genet Couns ; 25(3): 349-51, 2014.

Article in En | MEDLINE | ID: mdl-25365860

Subject(s)

Abnormalities, Multiple/diagnosis; Abnormalities, Multiple/genetics; Chromosome Disorders/diagnosis; Chromosome Disorders/genetics; Congenital Abnormalities/diagnosis; Congenital Abnormalities/genetics; Holoprosencephaly/diagnosis; Holoprosencephaly/genetics; Nose/abnormalities; Trisomy/diagnosis; Trisomy/genetics; Chromosomes, Human, Pair 13/genetics; Fatal Outcome; Humans; Infant, Newborn; Male; Phenotype; Trisomy 13 Syndrome

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Database: MEDLINE Main subject: Congenital Abnormalities / Trisomy / Abnormalities, Multiple / Nose / Holoprosencephaly / Chromosome Disorders Limits: Humans / Male / Newborn Language: En Year: 2014 Type: Article

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