Partial trisomy of 11 and 22 due to familial translocation t(11;22) (q23;q11), inherited in three generations
- 1 January 1979
- journal article
- research article
- Published by Springer Nature in Human Genetics
- Vol. 51 (3) , 349-355
- https://doi.org/10.1007/bf00283408
Abstract
No abstract availableThis publication has 11 references indexed in Scilit:
- The problem of partial trisomy 22 reconsideredHuman Genetics, 1978
- Cat Eye SyndromeAmerican Journal of Diseases of Children, 1977
- Partial trisomy 22: A recognizable syndromeClinical Genetics, 1977
- Familial translocation with partial trisomy of 13 and 22: evidence that specific regions of chromosomes 13 and 22 are responsible for the phenotype of each trisomy.Journal of Medical Genetics, 1977
- 47,XY,+der(11;22)(q23;q12) following balanced translocation t(11;22)(q23;q12)matHuman Genetics, 1977
- The Problem of Trisomy 22Clinical Pediatrics, 1976
- [Trisomy 11q. Individualization of a new syndrome].1975
- A (17;22) translocation, balanced, 46 chromosomesCytogenetic and Genome Research, 1975
- SATELLITE STAINING OF HUMAN CHROMOSOMESThe Lancet, 1974
- An Inherited Small Extra Chromosome: A Mother with 46,XX,t(17;22) (p1;q1) and a Son with 47,XY,+der(22) matJournal of Medical Genetics, 1973