Found: 5
Select item for more details and to access through your institution.
Alu-specific microhomology-mediated deletions in CDKL5 in females with early-onset seizure disorder.
- Published in:
- Neurogenetics, 2009, v. 10, n. 4, p. 363, doi. 10.1007/s10048-009-0195-z
- By:
- Publication type:
- Article
CHARGE Association: An update and review for the primary ...
- Published in:
- Clinical Pediatrics, 1998, v. 37, n. 3, p. 159, doi. 10.1177/000992289803700302
- By:
- Publication type:
- Article
The spectrum of clinical features in CHARGE syndrome.
- Published in:
- Clinical Genetics, 1986, v. 29, n. 4, p. 298, doi. 10.1111/j.1399-0004.1986.tb01258.x
- By:
- Publication type:
- Article
Usher syndrome: An otoneurologic study.
- Published in:
- Laryngoscope, 1989, v. 99, n. 1, p. 73, doi. 10.1288/00005537-198901000-00014
- By:
- Publication type:
- Article
Usher syndrome: Clinical findings and gene localization studies.
- Published in:
- Laryngoscope, 1989, v. 99, n. 1, p. 66, doi. 10.1288/00005537-198901000-00013
- By:
- Publication type:
- Article