Absence of detectable chromosomal and mo
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Litz, Craig E. ;Taylor, Kimberly A. ;Qiu, J. S. ;Pescovitz, Ora H. ;De Martinvil
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Article
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1988
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John Wiley and Sons
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English
β 877 KB
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.