Works matching IS 20908571 AND DT 2016 AND VI 5 AND IP 2
Results: 5
Angiotensin-converting enzyme insertion/deletion polymorphism in an Egyptian cohort of hypertrophic cardiomyopathy.
- Published in:
- Middle East Journal of Medical Genetics, 2016, v. 5, n. 2, p. 65, doi. 10.1097/01.MXE.0000484368.11655.d4
- By:
- Publication type:
- Article
Evaluation of telomerase activity in lymphoproliferative disorders.
- Published in:
- Middle East Journal of Medical Genetics, 2016, v. 5, n. 2, p. 60, doi. 10.1097/01.MXE.0000484371.78522.fd
- By:
- Publication type:
- Article
Chromosome 17q duplication associated with 21q telomeric deletion in a female patient with multiple congenital anomalies.
- Published in:
- Middle East Journal of Medical Genetics, 2016, v. 5, n. 2, p. 54, doi. 10.1097/01.MXE.0000484367.43852.26
- By:
- Publication type:
- Article
Genetic diagnosis of Prader-Willi syndrome.
- Published in:
- Middle East Journal of Medical Genetics, 2016, v. 5, n. 2, p. 45, doi. 10.1097/01.MXE.0000484369.78928.9e
- By:
- Publication type:
- Article
Pallister-Killian syndrome with fibular hypoplasia: a novel clinical manifestation.
- Published in:
- Middle East Journal of Medical Genetics, 2016, v. 5, n. 2, p. 41, doi. 10.1097/01.MXE.0000484370.71282.15
- By:
- Publication type:
- Article