An unusual case of Bardet-Biedl syndrome presenting with type 1 diabetes mellitus.
- Published in:
- Middle East Journal of Medical Genetics, 2012, v. 1, n. 2, p. 85, doi. 10.1097/01.MXE.0000414808.08492.ec
- By:
- Publication type:
- Article
Works matching IS 20908571 AND DT 2012 AND VI 1 AND IP 2
Results: 6
1
2
GJB2 gene mutations in Syrians with sensorineural hearing loss.
- Published in:
- Middle East Journal of Medical Genetics, 2012, v. 1, n. 2, p. 80, doi. 10.1097/01.MXE.0000414811.94762.bb
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- Publication type:
- Article
3
Cytokinesis-blocked micronucleus assay in a group of Egyptian patients with Fanconi anemia.
- Published in:
- Middle East Journal of Medical Genetics, 2012, v. 1, n. 2, p. 76, doi. 10.1097/01.MXE.0000414809.51187.d6
- By:
- Publication type:
- Article
4
Novel truncating mutation in the CTNS gene in an Egyptian family with cases of infantile nephropathic cystinosis and congenital heart malformations.
- Published in:
- Middle East Journal of Medical Genetics, 2012, v. 1, n. 2, p. 71, doi. 10.1097/01.MXE.0000414810.01450.3c
- By:
- Publication type:
- Article
5
Definition of the phenotypic spectrum of Temtamy preaxial brachydactyly syndrome associated with autosomal recessive CHYS1 mutations.
- Published in:
- Middle East Journal of Medical Genetics, 2012, v. 1, n. 2, p. 64, doi. 10.1097/01.MXE.0000414918.78299.94
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- Publication type:
- Article
6
Genetic polymorphism studies in humans.
- Published in:
- Middle East Journal of Medical Genetics, 2012, v. 1, n. 2, p. 57, doi. 10.1097/01.MXE.0000415225.85003.47
- By:
- Publication type:
- Article