A case of interstitial deletion of 10q25.2----q26.1.
- 1 January 1989
- journal article
- case report
- Published by BMJ in Journal of Medical Genetics
- Vol. 26 (1) , 58-60
- https://doi.org/10.1136/jmg.26.1.58
Abstract
A de novo interstitial deletion of chromosome 10, del(10)(pter----q25.2::q26.1----qter), was detected in a newborn female with facial anomalies, failure to thrive, and subsequent developmental delay. This case is compared with 10 previous reports of monosomy 10q within the q25----qter region.Keywords
This publication has 19 references indexed in Scilit:
- A further case of monosomy 10qterClinical Genetics, 2008
- Monosomy 10qter due to a balanced maternal translocation: t(10;8)(q23;p23)Clinical Genetics, 2008
- Behaviour disorder in monosomy 10qter.Journal of Medical Genetics, 1987
- Terminal deletion of the long arm of chromosome 10.Journal of Medical Genetics, 1986
- 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
- SC phocomelia syndrome, premature centromere separation, and congenital cranial nerve paralysis in two sisters, one with malignant melanomaAmerican Journal of Medical Genetics, 1986
- Deletions of the long arm of chromosome 10American Journal of Medical Genetics, 1985
- The syndrome of Yunis and Varón—report of a further caseAmerican Journal of Medical Genetics, 1983
- Is there a monosomy 10qter syndrome?Clinical Genetics, 1982
- CLEIDOCRANIAL DYSOSTOSISAmerican Journal of Roentgenology, 1974