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EPIDEMIOLOGIC-STUDY OF DOWNS-SYNDROME IN DENMARK, INCLUDING FAMILY STUDIES OF CHROMOSOMES AND DNA MARKERS
Author(s): MIKKELSEN M, HALLBERG A, POULSEN H, FRANTZEN M, HANSEN J, PETERSEN MB
Source: DEVELOPMENTAL BRAIN DYSFUNCTION    Volume: 8    Issue: 1    Pages: 4-12    Published: JAN-FEB 1995  
Times Cited: 27     References: 48     
Abstract: All cases of Down's syndrome in Demmark born or aborted after prenatal diagnosis between January 1, 1990 and March 31, 1993 were registered. In a population of 5 millions and a birth rate of about 60,000-65,000 births per year, 207 liveborn and 159 fetuses aborted after prenatal diagnosis were registered. Ten cases of translocation or isochromosome 21 (4.8%) and 7 mosaics (3.4%) were found among the newborn infants. All available families with a trisomic child (119 newborn infants) were studied by DNA markers to identify the origin of the extra chromosome. In 8.4% the extra chromosome was paternal. In cases of maternal meiosis I and II errors maternal age was increased (mean 30.6 years). In paternal cases and mitotic cases no maternal age effect was observed (mean 28.0 and 26.8 years). The sex ratio was distorted especially in paternal errors and maternal meiosis II errors.
Document Type: Article
Language: English
Reprint Address: MIKKELSEN, M (reprint author), JOHN F KENNEDY INST, DEPT MED GENET, 7, GIL LANDEVEJ, DK-2600 GLOSTRUP, DENMARK
Addresses:
1. CYTOGENET CENT REGISTER, RISSKOV, DENMARK
Publisher: KARGER, ALLSCHWILERSTRASSE 10, CH-4009 BASEL, SWITZERLAND
Subject Category: Developmental Biology; Neurosciences
IDS Number: TD388
ISSN: 1019-5815
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