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CHROMOSOMAL ENDOREDUPLICATION IN A CASE OF TURNER'S SYNDROME WITH 46/XX KARYOTYPE

✍ Scribed by BOCZKOWSKI, K


Book ID
122908334
Publisher
The Lancet
Year
1965
Tongue
English
Weight
328 KB
Volume
285
Category
Article
ISSN
0140-6736

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Chromosome 14 maternal uniparental disom
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We investigated the parental origin of the extra chromosome 14 and of the two chromosomes 14 of the euploid cell line, in a case of fetal mosaicism 46,XX/47,XX+14 diagnosed at amniocentesis. Molecular analysis of five polymorphic loci of the short tandem repeat type was performed. Markers D14S43 and