Partial trisomy 11,46,XX,-3,-20,+der3,+der20,t(3:11:20), resulting from a complex maternal rearrangement of chromosomes 3, 11, 20
- 1 January 1976
- journal article
- research article
- Published by Springer Nature in Human Genetics
- Vol. 31 (2) , 219-225
- https://doi.org/10.1007/bf00296149
Abstract
Clinical findings of partial trisomy 11p are described in a patient bearing t(3;11;20) (p13;p11;q13). The translocation was present in balanced form in her mother (46,XX)t(3;11;20)(p13;p11;q13).This publication has 14 references indexed in Scilit:
- Complex five-break rearrangementClinical Genetics, 2008
- Familial balanced (7;11;21)translocation and Down's syndrome in two siblingsClinical Genetics, 1975
- Partial trisomy 11 in a child resulting from a complex maternal rearrangement of chromosomes 11, 12 and 13Published by Springer Nature ,1974
- Possible complex translocation t(9; 14; 13)(q12;pl?;q31) in mother of a child with 9p-trisomy syndromeHuman Genetics, 1974
- [Complexe de novo rearrangement involving 4 chromosomes in a newborn infant].1973
- [Crying cat disease associated with complex chromosome rearrangement in a dizygotic twin].1973
- Partial trisomy of chromosome 11: a case report.1973
- A pericentric inversion, 5p–q+, and additional complex rearrangements in a case of cri-du-chat syndromeCytogenetic and Genome Research, 1971
- A complex familial translocation involving chromosomes 5, 9 and 13Cytogenetic and Genome Research, 1970
- A case of multiple chromosomal rearrangements with persistence of foetal haemoglobinCytogenetic and Genome Research, 1968