Absence of detectable chromosomal and molecular abnormalities in monozygotic twins discordant for the Wiedemann-Beckwith syndrome.
Am J Med Genet
; 30(3): 821-33, 1988 Jul.
Article
em En
| MEDLINE
| ID: mdl-3189402
ABSTRACT
Monozygotic twins discordant for the Wiedemann-Beckwith syndrome (WBS) were studied by cytogenetic and molecular methods to determine if a genetic lesion could be detected in the affected child. Probes known to be localized on the short arm of chromosome 11 and a low copy-repetitive probe were used. No genetic lesions could be ascertained in normal or affected tissue obtained from the WBS twin.
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Base de dados:
MEDLINE
Assunto principal:
Síndrome de Beckwith-Wiedemann
/
Doenças em Gêmeos
Limite:
Female
/
Humans
/
Infant
Idioma:
En
Revista:
Am J Med Genet
Ano de publicação:
1988
Tipo de documento:
Article