Found: 2
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FOXP1 haploinsufficiency: Phenotypes beyond behavior and intellectual disability?
- Published in:
- American Journal of Medical Genetics. Part A, 2017, v. 173, n. 12, p. 3172, doi. 10.1002/ajmg.a.38462
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- Publication type:
- Article
Pelger-huet anomaly and a mild skeletal phenotype secondary to mutations in LBR.
- Published in:
- American Journal of Medical Genetics. Part A, 2013, v. 161A, n. 8, p. 2066, doi. 10.1002/ajmg.a.36019
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- Publication type:
- Article