The de novo chromosome 16 translocations of two patients with abnormal phenotypes (mental retardation and epilepsy) disrupt the A2BP1 gene
- 18 May 2004
- journal article
- case report
- Published by Springer Science and Business Media LLC in Journal of Human Genetics
- Vol. 49 (6), 308-311
- https://doi.org/10.1007/s10038-004-0145-4
Abstract
Journal of Human Genetics, official journal of the Japan Society of Human Genetics, publishes original articles and reviews on all aspects of human genetics, including medical genetics and genomicsKeywords
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