Works matching IS 20908571 AND DT 2018 AND VI 7 AND IP 1

Results: 9

The scope of orodental genetics: Erratum.
Published in:
Middle East Journal of Medical Genetics, 2018, v. 7, n. 1, p. 50, doi. 10.4103/2090-8571.228080
Publication type:
Article
Cornelia de Lange syndrome type 5: report of two new cases.
Published in:
Middle East Journal of Medical Genetics, 2018, v. 7, n. 1, p. 46, doi. 10.4103/MXE.MXE_2_17
By:
- de Gabory, Claire Le Taillandier;
- Abou-Sleymane, Gretta;
- Stora, Samantha;
- Obeid, Marc;
- Mikael, David;
- Megarbane, André
Publication type:
Article
The CDKN2BAS polymorphism rs2891168 is associated with increased risk of myocardial infarction in a Saudi Arabian population.
Published in:
Middle East Journal of Medical Genetics, 2018, v. 7, n. 1, p. 39, doi. 10.4103/MXE.MXE_6_17
By:
- Hadi Al-Ama, Mohmd N. A.;
- Elmgeed Ahmed, Ahmed A.;
- Awan, Zuhair A.;
- Ajabnoor, Ghada M. A.;
- Alshali, Khalid Z.;
- Ajabnoor, Mohammad A. M.
Publication type:
Article
Molecular characterization of patients with clinical suspicion of 22q11.2 deletion syndrome.
Published in:
Middle East Journal of Medical Genetics, 2018, v. 7, n. 1, p. 32, doi. 10.4103/MXE.MXE_3_18
By:
- Abd El-Ghany, Hoda M.;
- Mekkawy, Mona K.;
- Helmy, Nevin A.;
- Eid, Ola M.;
- Elruby, Mona O.;
- Refaat, Khaled M.;
- El-Saiedi, Sonia A.;
- Fayez, Alaaeldeen G.;
- Samy, Rania M.
Publication type:
Article
Screening for parental mitotic nondisjunction as a cause of fetal aneuploidy.
Published in:
Middle East Journal of Medical Genetics, 2018, v. 7, n. 1, p. 26, doi. 10.4103/MXE.MXE_1_18
By:
- Hussen, Dalia F.;
- Hammad, Saida A.;
- Refaat, Khaled M.;
- Ashaat, Engy A.;
- Gaber, Khaled R.;
- Aglan, Mona S.;
- Otaify, Ghada A.;
- Abdel Ghany, Asia E.;
- Temtamy, Samia A.
Publication type:
Article
The covariant CDKN2A/B rs10811661 (C/T) gene polymorphism is associated with increased risk of type 2 diabetes mellitus in a Saudi Arabian population.
Published in:
Middle East Journal of Medical Genetics, 2018, v. 7, n. 1, p. 19, doi. 10.4103/MXE.MXE_5_17
By:
- Ajabnoor, Mohammad A. M.;
- Elmgeed Ahmed, Ahmed A.;
- Hadi Al-Ama, Mohmd N. A.;
- Alshali, Khalid Z.;
- Ajabnoor, Ghada M. A.
Publication type:
Article
Assessment of phenotype and genotype in neuronal ceriod lipofuscinosis among Egyptian children.
Published in:
Middle East Journal of Medical Genetics, 2018, v. 7, n. 1, p. 11, doi. 10.4103/MXE.MXE_4_17
By:
- Megahed, Hisham;
- Fateen, Ekram;
- El-Gawaby, Hamed;
- Galal, Nadia;
- Hindawy, Amina
Publication type:
Article
Risk factors in obese Egyptian women with polycystic ovary syndrome.
Published in:
Middle East Journal of Medical Genetics, 2018, v. 7, n. 1, p. 7, doi. 10.4103/MXE.MXE_1_17
By:
- Shousha, Wafaa G.;
- Zaki, Moushira E.;
- El Bassyouni, Hala T.;
- Abdo, Sara M.;
- Mohamed, Salwa M.
Publication type:
Article
Clinical genetics revisited: effect of new techniques (next-generation sequencing, comparative genomic hybridization) on previous diagnoses.
Published in:
Middle East Journal of Medical Genetics, 2018, v. 7, n. 1, p. 1, doi. 10.4103/MXE.MXE_3_17
By:
- Mégarbané, Andre
Publication type:
Article