13q- syndrome. Family study.
- 1 December 1977
- journal article
- research article
- Published by BMJ in Archives of Disease in Childhood
- Vol. 52 (12) , 972-974
- https://doi.org/10.1136/adc.52.12.972
Abstract
A patient is described who had a deletion involving the long arm of chromosome number 13. The mother and 4 of 7 living sibs showed a balanced translocation from the long arm of a number 13 chromosome to the long arm of a number 3 chromosome. We stress the importance of investigating the families of children with chromosomal defects.This publication has 9 references indexed in Scilit:
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- Partial monosomy 13 as the result of a balanced translocation 3/13 patHuman Genetics, 1975
- New Chromosomal SyndromesArchives of Pediatrics & Adolescent Medicine, 1975
- [Partial 13 trisomy by maternal 46, XX, t (3; 13) (p 26; q 21) translocation].1974
- Henoch-Schoenlein SyndromePediatric Clinics of North America, 1972
- The 13q- deletion syndrome.Journal of Medical Genetics, 1971
- The 13q-deletion syndrome.1969
- Pulmonary Hemorrhage and Death Complicating Anaphylactoid PurpuraSouthern Medical Journal, 1967
- THE SCHÖNLEIN-HENOCH SYNDROME (ANAPHYLACTOID PURPURA)QJM: An International Journal of Medicine, 1948