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- W2113368105 abstract "A minute familial translocation t(10;16) (q26;p13.1) was detected in a family with 6 affected children in 2 generations and 9 carriers in 3 generations. This apparently unique translocation is associated with a deleterious syndrome which includes fetal hydrops, ascites, complex congenital heart defect, psychomotor retardation, failure to thrive, hypotonia, narrow palpebral fissures, abnormally modeled, apparently low-set ears, cleft palate, thumb abnormalities, hypogenitalism, inguinal hernia, and sparse hair. All children of known or presumed carriers have been either balanced or unbalanced carriers of this translocation." @default.
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- W2113368105 date "1991-01-01" @default.
- W2113368105 modified "2023-10-14" @default.
- W2113368105 title "A familial MCA/MR syndrome due to translocation t(10;16)(q26;p13.1): Report of six cases" @default.
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- W2113368105 doi "https://doi.org/10.1002/ajmg.1320380102" @default.
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