Found: 4
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Expansion of the Variable Expression of Muenke Syndrome: Hydrocephalus without Craniosynostosis.
- Published in:
- American Journal of Medical Genetics. Part A, 2016, v. 170, n. 12, p. 3189, doi. 10.1002/ajmg.a.37951
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- Publication type:
- Article
Erratum to: Germline Mutations in NKX2-5, GATA4, and CRELD1 are Rare in a Mexican Sample of Down Syndrome Patients with Endocardial Cushion and Septal Heart Defects.
- Published in:
- 2015
- By:
- Publication type:
- Erratum
Histone deacetylases modulate resistance to the therapy in lung cancer.
- Published in:
- Frontiers in Genetics, 2022, v. 13, p. 1, doi. 10.3389/fgene.2022.960263
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- Publication type:
- Article
Molecular analysis of the PAX8 gene in a sample of Mexican patients with primary congenital hypothyroidism: identification of the recurrent p.Arg31His mutation.
- Published in:
- Clinical Endocrinology, 2012, v. 76, n. 1, p. 148, doi. 10.1111/j.1365-2265.2011.04153.x
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- Publication type:
- Article