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Works matching IS 20908571 AND DT 2016 AND VI 5 AND IP 2

Results: 5

1

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:

Kassem, Heba Sh.;
Algendy, Sherif A.;
Azer, Remon S.;
Magdy, Gehan;
Moharem-Elgamal, Sarah;
Ayad, Maha S.;
Elguindy, Ahmed;
Abdelghany, Besra S.;
Yacoub, Magdi H.

Publication type:

Article

2

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:

Zayed, Shahera A.;
Mansour, Osman M.;
Kholoussi, Naglaa M.;
Razik, Heba A.;
Kh, Amr;
Maksoud, Sohier A.;
Raouf, Haiam Abdel;
Ismail, Somai;
Kandil, Raina

Publication type:

Article

3

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:

Mekkawy, Mona K.;
Mazen, Inas M.;
Kamel, Alaa K.;
Mahmoud, Wael;
Mohamed, Amal M.

Publication type:

Article

4

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:

Khedr, Azzah A.;
Meguid, Nagwa A.;
Mohamed, Amal M.;
Ismail, Suzan R.;
Nazmy, Nahla A.;
Hassan, Heba A.;
Essawi, Mona L.

Publication type:

Article

5

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:

Sadik, Doaa I.;
Al-Hathal, Muneef;
Ghareeb, Tarek M.;
Abulhasan, Sawsan J.;
Bastaki, Laila A.

Publication type:

Article