Progressive osseous heteroplasia (POH): an Egyptian patient.
- Published in:
- 2010
- By:
- Publication type:
- Case Study
Works matching IS 11108630 AND DT 2010 AND VI 11 AND IP 1
Results: 10
1
2
Educational case of the issue.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2010, v. 11, n. 1, p. 91
- By:
- Publication type:
- Article
3
Gene polymorphisms of TNF-α and IL-10 related to rheumatic heart disease.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2010, v. 11, n. 1, p. 33
- By:
- Publication type:
- Article
4
Genomics in health and disease.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2010, v. 11, n. 1, p. 11
- By:
- Publication type:
- Article
5
Genetic study of congenital limb anomalies among Egyptian children.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2010, v. 11, n. 1, p. 47
- By:
- Publication type:
- Article
6
Corpus callosum defect with dilated lateral ventricles and an occipital cyst in an Egyptian child with Diamond-Blackfan anemia.
- Published in:
- 2010
- By:
- Publication type:
- Case Study
7
Severe congenital neutropenia (Kostmann Syndrome).
- Published in:
- Egyptian Journal of Medical Human Genetics, 2010, v. 11, n. 1, p. 1
- By:
- Publication type:
- Article
8
Peters' plus syndrome in an Egyptian patient with some unusual features.
- Published in:
- 2010
- By:
- Publication type:
- Case Study
9
Common MEFV mutations in Egyptian patients with familial Mediterranean fever.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2010, v. 11, n. 1, p. 59
- By:
- Publication type:
- Article
10
L-Carnitine ameliorates the iron mediated DNA degradation in peripheral leukocytes of β- thalassemic children.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2010, v. 11, n. 1, p. 17
- By:
- Publication type:
- Article