Cytogenetic studies of a family with trisomy 21 mosaicism in two successive generations as the cause of Down's syndrome
- 1 January 1982
- journal article
- research article
- Published by Springer Nature in Human Genetics
- Vol. 60 (2) , 202-204
- https://doi.org/10.1007/bf00569714
Abstract
No abstract availableThis publication has 10 references indexed in Scilit:
- Trisomy 21 mosaicism in two successive generations in a family.Journal of Medical Genetics, 1980
- Reproduction in a woman with mosaicism.Journal of Medical Genetics, 1978
- Reproduction in a woman with low percentage t(21q21q) mosaicism.Journal of Medical Genetics, 1977
- Parental mosaicism as a cause of down syndrome: A report of 46,XX/46,XX, −21,+t(21q21q) mother and 46,XY,+21,+t(21q21q) childThe Journal of Pediatrics, 1977
- Trisomy 21 mosaicism in a woman with two children with trisomy 21 Down's syndromeJournal of Medical Genetics, 1974
- INVESTIGATION OF 142 MOSAIC MONGOLS AND MOSAIC PARENTS OF MONGOLS; CYTOGENETIC ANALYSIS AND MATERNAL AGE AT BIRTHJournal of Intellectual Disability Research, 1974
- Paternal trisomy 21 mosaicism and Down's anomalyHumangenetik, 1973
- A simple technique for demonstrating centromeric heterochromatinExperimental Cell Research, 1972
- A RAPID BANDING TECHNIQUE FOR HUMAN CHROMOSOMESThe Lancet, 1971