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Works matching IS 20908571 AND DT 2013 AND VI 2 AND IP 2

Results: 5

1

A boy with hand anomalies similar to those documented with prenatal misoprostol exposure.

Published in:

Middle East Journal of Medical Genetics, 2013, v. 2, n. 2, p. 58, doi. 10.1097/01.MXE.0000430778.37375.13

By:

Baynam, Gareth S.;
Gonzalez, Claudette;
Temtamy, Samia A.

Publication type:

Article

2

Molecular diagnosis of myotonic dystrophy type 1 in Egyptian patients.

Published in:

Middle East Journal of Medical Genetics, 2013, v. 2, n. 2, p. 55, doi. 10.1097/01.MXE.0000430776.91633.a4

By:

Effat, Laila K.;
Abdalla, Hoda;
Ismail, Somia;
El-Hadidi, Iman;
Helmi, Dalia;
Fahmi, Nagia;
Afifi, Hanan H.

Publication type:

Article

3

Association of CALHM1 gene polymorphism with late-onset Alzheimer disease.

Published in:

Middle East Journal of Medical Genetics, 2013, v. 2, n. 2, p. 50, doi. 10.1097/01.MXE.0000430777.29752.3a

By:

Gharesouran, Jalal;
Rezazadeh, Maryam;
Ghojazadeh, Morteza;
Mohaddes Ardebili, Seiied Mojtaba

Publication type:

Article

4

Evaluation of the in-vitro protective effect of plant extract (astaxanthin) on chromosomal breakage in Fanconi anemia cell culture.

Published in:

Middle East Journal of Medical Genetics, 2013, v. 2, n. 2, p. 45, doi. 10.1097/01.MXE.0000430775.91633.7f

By:

Eid, Maha M.;
Temtamy, Sami A.;
Soliman, Engy S.;
Shehab, Marwa I.;
Abd Alaziz, Sami H.;
Baraka, Dina H.;
Hamdy, Mona

Publication type:

Article

5

Woodhouse-Sakati syndrome in six Kuwaiti families.

Published in:

Middle East Journal of Medical Genetics, 2013, v. 2, n. 2, p. 39, doi. 10.1097/01.MXE.0000430774.84009.80

By:

Bastaki, Laila;
Al-Wadaani, Amal;
Gouda, Sayed;
Al-Aboud, Hayat;
Elshafey, Alaa

Publication type:

Article