Found: 4
Select item for more details and to access through your institution.
20 ans après: a second mutation in MAOA identified by targeted high-throughput sequencing in a family with altered behavior and cognition.
- Published in:
- European Journal of Human Genetics, 2014, v. 22, n. 6, p. 776, doi. 10.1038/ejhg.2013.243
- By:
- Publication type:
- Article
12p13.33 microdeletion including ELKS/ERC1, a new locus associated with childhood apraxia of speech.
- Published in:
- European Journal of Human Genetics, 2013, v. 21, n. 1, p. 82, doi. 10.1038/ejhg.2012.116
- By:
- Publication type:
- Article
A new family with an SLC9A6 mutation expanding the phenotypic spectrum of Christianson syndrome.
- Published in:
- American Journal of Medical Genetics. Part A, 2016, v. 170A, n. 8, p. 2103, doi. 10.1002/ajmg.a.37765
- By:
- Publication type:
- Article
Expanding the clinical phenotype of patients with a ZDHHC9 mutation.
- Published in:
- American Journal of Medical Genetics. Part A, 2014, v. 164A, n. 3, p. 789, doi. 10.1002/ajmg.a.36348
- By:
- Publication type:
- Article