NRXN1 deletion syndrome; phenotypic and penetrance data from 34 families
- Resource Type
- Article
- Authors
- Al Shehhi, Maryam; Forman, Eva B.; Fitzgerald, Jacqueline E.; McInerney, Veronica; Krawczyk, Janusz; Shen, Sanbing; Betts, David R.; Ardle, Linda Mc; Gorman, Kathleen M.; King, Mary D.; Green, Andrew; Gallagher, Louise; Lynch, Sally A.
- Source
- In European Journal of Medical Genetics March 2019 62(3):204-209
- Subject
- Language
- ISSN
- 1769-7212