Compound heterozygote CDK5RAP2 mutations in a Guatemalan/Honduran child with autosomal recessive primary microcephaly, failure to thrive and speech delay
- Resource Type
- Academic Journal
- Source
- American Journal Of Medical Genetics - A. Jun 01, 2015 167(6):1414-1417
- Subject
- Language
- English
- ISSN
- 1552-4825