Works matching IS 20908571 AND DT 2013 AND VI 2 AND IP 2
Results: 5
A boy with hand anomalies similar to those documented with prenatal misoprostol exposure.
- Published in:
- Middle East Journal of Medical Genetics, 2013, v. 2, n. 2, p. 58, doi. 10.1097/01.MXE.0000430778.37375.13
- By:
- Publication type:
- Article
Molecular diagnosis of myotonic dystrophy type 1 in Egyptian patients.
- Published in:
- Middle East Journal of Medical Genetics, 2013, v. 2, n. 2, p. 55, doi. 10.1097/01.MXE.0000430776.91633.a4
- By:
- Publication type:
- Article
Association of CALHM1 gene polymorphism with late-onset Alzheimer disease.
- Published in:
- Middle East Journal of Medical Genetics, 2013, v. 2, n. 2, p. 50, doi. 10.1097/01.MXE.0000430777.29752.3a
- By:
- Publication type:
- Article
Evaluation of the in-vitro protective effect of plant extract (astaxanthin) on chromosomal breakage in Fanconi anemia cell culture.
- Published in:
- Middle East Journal of Medical Genetics, 2013, v. 2, n. 2, p. 45, doi. 10.1097/01.MXE.0000430775.91633.7f
- By:
- Publication type:
- Article
Woodhouse-Sakati syndrome in six Kuwaiti families.
- Published in:
- Middle East Journal of Medical Genetics, 2013, v. 2, n. 2, p. 39, doi. 10.1097/01.MXE.0000430774.84009.80
- By:
- Publication type:
- Article