Terminal deletion of chromosome 10q26 due to a paternal translocation {(7;10)(q36;q26)}
- 15 December 1991
- journal article
- Published by Wiley in American Journal of Medical Genetics
- Vol. 41 (4) , 534-536
- https://doi.org/10.1002/ajmg.1320410434
Abstract
No abstract availableThis publication has 10 references indexed in Scilit:
- Terminal deletion of the long arm of chromosome 10: Case report and review of the literatureAmerican Journal of Medical Genetics, 1989
- Chromosome 10qter deletion syndrome: A review and report of three new casesAmerican Journal of Medical Genetics, 1989
- Severe mental retardation in six generations of a large South African family carrying a translocation t(6;10)(q27;q25.2).Journal of Medical Genetics, 1986
- Deletions of the long arm of chromosome 10American Journal of Medical Genetics, 1985
- Familial reciprocal translocation, t(2;10)(p24;q26), resulting in duplication 2p and deletion 10qClinical Genetics, 1982
- A severely retarded male with deletion of chromosomes 15 (pter leads to q13) and 10 (q 26 leads to qter).Journal of Medical Genetics, 1982
- Phenotype associated with ring 10 chromosome: Report of patient and review of literatureAmerican Journal of Medical Genetics, 1981
- Ring chromosome 10: 46,XX,r(10)(p15->q26)Journal of Medical Genetics, 1980
- Ring chromosome 10 Associated with multiple congenital malformationsHuman Genetics, 1979
- Ring 10 chromosome: 46,XX,r10(p15q26)Human Genetics, 1978