A further case of monosomy 10qter
- 28 June 2008
- journal article
- research article
- Published by Wiley in Clinical Genetics
- Vol. 24 (3) , 216-219
- https://doi.org/10.1111/j.1399-0004.1983.tb02242.x
Abstract
A child with a terminal deletion of chromosome 10 (q26) is described. A comparison of the phenotypic and cytogenetic features is made in the 5 reported cases of monosomy 10qter. No phenotypic features are found sufficiently characteristic to delineate a syndrome. Enzymatic activities for PGAMA [phosphoglycerate mutase] and GOT1 [glutamate oxaloacetate transaminase] were normal.Keywords
This publication has 7 references indexed in Scilit:
- A further case of monosomy 10qterClinical Genetics, 2008
- Monosomy 10qter due to a balanced familial translocation: t(10;16)(q25.2;q24)Clinical Genetics, 2008
- ASSIGNMENT OF PHOSPHOGLYCERATE MUTASE (PGAMA) TO HUMAN-CHROMOSOME .10. REGIONAL MAPPING OF GOTI AND PGAMA TO SUBBANDS 10Q26.1 (OR Q25.3)1982
- Is there a monosomy 10qter syndrome?Clinical Genetics, 1982
- Monosomy 10 qterHuman Genetics, 1979
- Partial deletion 10qHuman Genetics, 1978