Complex translocation t(9;21)(9;22)(q12p13)(q12q11) in the family of a child with 9p trisomy syndrome
- 1 January 1976
- journal article
- research article
- Published by Springer Nature in Human Genetics
- Vol. 33 (1) , 73-76
- https://doi.org/10.1007/bf00447289
Abstract
A case of partial trisomy 9 is described in a mentally retarded and dysmorphic child, confirming that this chromosome unbalance results in a characteristic clinical entity. This trisomy arose through aberrant segregation of translocation chromosome during meiosis in the patient's mother, who is a balanced heterozygote for a complex translocation involving chromosomes 9, 21 and 22. The phenotypically normal sister of the propositus is also carrier of the same complex translocation.This publication has 6 references indexed in Scilit:
- Observations on specific Giemsa staining of the Y and on selective oil destaining of the chromosomesHumangenetik, 1975
- Trisomy 9p in a patient with a de novo 9/15 translocationClinical Genetics, 1975
- Physical and mental defect of chromosomal origin in four individuals of the same family. Trisomy for the short arm of 9Clinical Genetics, 1975
- Possible complex translocation t(9; 14; 13)(q12;pl?;q31) in mother of a child with 9p-trisomy syndromeHuman Genetics, 1974
- Nouveau système de marquage chromosomique: les bandes TChromosoma, 1973