NRXN1 Deletion in Two Twins' Genotype and Phenotype: A Clinical Case and Literature Review.
- Resource Type
- Article
- Source
- Children; May2022, Vol. 9 Issue 5, p698-N.PAG, 9p
- Subject
COGNITION disorder risk factors GENETIC mutation SEQUENCE analysis CRANIOFACIAL abnormalities TWINS GENETIC testing GENES GENOTYPES CHILD psychopathology GENOMICS PHENOTYPES CHILDREN - Language
- ISSN
- 22279067