A case of apparent trisomy 21 without the Down's syndrome phenotype.

Avramopoulos, D; Kennerknecht, I; Barbi, G; Eckert, D; Delabar, J M; Maunoury, C; Hallberg, A; Petersen, M B

Avramopoulos, D; Kennerknecht, I; Barbi, G; Eckert, D; Delabar, J M; Maunoury, C; Hallberg, A; Petersen, M B.

Affiliation

Avramopoulos D; Department of Genetics, Aghia Sophia Children's Hospital, Athens, Greece.

J Med Genet ; 34(7): 597-600, 1997 Jul.

Article in En | MEDLINE | ID: mdl-9222973

Subject(s)

Down Syndrome/genetics; Down Syndrome/pathology; Female; Haemophilus Infections/complications; Haemophilus influenzae; Humans; In Situ Hybridization, Fluorescence; Infant, Newborn; Intellectual Disability/etiology; Meningitis, Bacterial/complications; Mosaicism/genetics; Phenotype

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Full text: 1 Collection: 01-internacional Health context: 3_ND Database: MEDLINE Main subject: Down Syndrome Type of study: Etiology_studies Limits: Female / Humans / Newborn Language: En Journal: J Med Genet Year: 1997 Document type: Article

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