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Tissue-specific mosaicism for trisomy 21 and congenital heart disease

โœ Scribed by Yuji Yokoyama; Kouji Narahara; Masahiro Kamada; Kazushiro Tsuji; Yoshiki Seino

Book ID
117163613
Publisher
Elsevier Science
Year
1992
Tongue
English
Weight
981 KB
Volume
121
Category
Article
ISSN
1097-6833

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A newborn infant born to consanguineous (first cousin) parents was noted to have complex congenital heart defect and minor anomalies suggestive of trisomy 18. Blood lymphocyte and skin fibroblast karyotypes were normal. He died in the neonatal period of postoperative complications. On interphase flu