Trisomy 9p and unusual translocation mongolism in siblings due to different 3:1 segregations of maternal translocation rcp(9;21)(p11;q11)
- 1 January 1978
- journal article
- research article
- Published by Springer Nature in Human Genetics
- Vol. 42 (3) , 251-256
- https://doi.org/10.1007/bf00291304
Abstract
Two sisters are described, each with a specific retardation syndrome due to a balanced reciprocal translocation 9p;21q in the mother. As a result of different 3:1 segregations, one of them has a trisomy 9p with all typical features; the other one reveals a typical Down's syndrome having an unusual translocation karyotype.This publication has 14 references indexed in Scilit:
- Trisomy 9p syndrome and XYY syndrome in siblingsClinical Genetics, 1977
- Trisomy 9p resulting from maternal 9/21 translocationHuman Genetics, 1976
- 47,+(9q-) in unrelated three children with plasma growth hormon deficiencyHuman Genetics, 1976
- Genetics of the +p9 syndromeHuman Genetics, 1976
- Reciprocal translocations in man. 3:1 Meiotic disjunction resulting in 47- or 45-chromosome offspring.Journal of Medical Genetics, 1975
- Familial translocation t(3p-;21q+) associated with both Down's and Sturge-Weber's syndrome in unbalanced stateHuman Genetics, 1975
- The G-banded prophase chromosomes of manHuman Genetics, 1975
- Analyse de la trisomie 9p par dénaturation ménagéePublished by Springer Nature ,1973
- Banding in Human Chromosomes treated with TrypsinNature New Biology, 1972
- Chromosomal interchanges in plantsThe Botanical Review, 1956