Proximal 15q monosomy.
Open Access
- 1 October 1982
- journal article
- Published by BMJ in Journal of Medical Genetics
- Vol. 19 (5), 393-394
- https://doi.org/10.1136/jmg.19.5.393-a
Abstract
No abstract availableThis publication has 7 references indexed in Scilit:
- 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
- CHROMOSOME-15 ABNORMALITIES AND THE PRADER-WILLI SYNDROME - A FOLLOW-UP REPORT OF 40 CASES1982
- Correspondence: Gonadal dysgenesis with 46,X,Xt(qter->p221:: p223->qter) karyotypeJournal of Medical Genetics, 1981
- Adjacent 2 meiotic disjunction. Report of a case resulting from a familial 13q;15q balanced reciprocal translocation and review of the literatureHuman Genetics, 1981
- Deletions of Chromosome 15 as a Cause of the Prader–Willi SyndromeNew England Journal of Medicine, 1981
- Reciprocal translocations: A way to predict the mode of imbalanced segregation by pachytene-diagram drawingHuman Genetics, 1980
- Reciprocal translocations in man. 3:1 Meiotic disjunction resulting in 47- or 45-chromosome offspring.Journal of Medical Genetics, 1975