Distal 11q monosomy. The typical 11q monosomy syndrome is due to deletion of subband 11q24.1
- 1 October 1986
- journal article
- research article
- Published by Wiley in Clinical Genetics
- Vol. 30 (4) , 255-260
- https://doi.org/10.1111/j.1399-0004.1986.tb00605.x
Abstract
In this paper we describe two new patients with distal 11q monosomy and precisely localize breakpoints using high resolution banding techniques. The findings in these two patients further contribute to the precise localization of the crucial band for 11q monosomy syndrome as being at 11q24.1. A very distal 11q24.2 deletion in the second patient resulted in a completely different phenotype.Keywords
This publication has 21 references indexed in Scilit:
- Partial deletion of long arm of chromosome 11: del (11) (q23)Clinical Genetics, 2008
- New anomalies found in the 11q- syndromeClinical Genetics, 2008
- Deletion of the long arm of chromosome 11 [46, XX, deI(11)(q24.1 → qter)]Clinical Genetics, 1984
- Ring-11 chromosome: Phenotype-karyotype correlation with deletions of 11qAmerican Journal of Medical Genetics, 1983
- Deletion of the long arm of chromosome 11, [del(11)(q23)]American Journal of Medical Genetics, 1982
- Das 11 q-SyndromKlinische Padiatrie, 1981
- Craniosynostosis and syndactyly: expanding the 11q-- chromosomal deletion phenotype.Journal of Medical Genetics, 1980
- DELETION OF THE LONG ARM OF CHROMOSOME 11 A Clinical EntityActa Paediatrica, 1979
- Partial deletion of long arm of chromosome 11[del(11)(q23)]: Jacobsen syndrome. Two new cases and review of the clinical findings.Journal of Medical Genetics, 1977
- Anomalies associated with partial deletion of long arm of chromosome 11The Journal of Pediatrics, 1975