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1.
Molecular characterization of NRXN1 deletions from 19,263 clinical microarray cases identifies exons important for neurodevelopmental disease expression.
Genet Med
; 19(1): 53-61, 2017 01.
Article
in English
| MEDLINE | ID: mdl-27195815
2.
Genetic analysis of patients with the Saethre-Chotzen phenotype.
Am J Med Genet
; 110(2): 136-43, 2002 Jun 15.
Article
in English
| MEDLINE | ID: mdl-12116251
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