Down syndrome with unusual familial translocation (1;21) . A case report
Sayee, R.; Thomas, I.M.
Annales de Genetique 36(3): 171-172
1993
ISSN/ISBN: 0003-3995 PMID: 8117064 Document Number: 405786
A case of t(1;21) in a 9-year-old female Down syndrome patient is reported. Her karyotype was 47, XX, t(1;21) (mat), +21. The father's karyotype was normal, while that of the mother was 46, XX, t(1;21). An amniotic fluid cell culture revealed a trisomy 21 and a t(1;21) in a male fetus. This is the first report of a familial case of trisomy 21 with t(1;21) from our country.
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