Zaki, Mohamed SamirA: search on Z-Library

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1

Blepharophimosisâptosisâintellectual disability syndrome: A report of nine Egyptian patients with further expansion of phenotypic and mutational spectrum

Zaki, Maha S., Otaify, Ghada A., Ismail, Samira, Issa, Mahmoud Y., ElâRuby, Mona O., Sadek, Abdelrahim A., Ashaat, Engy A., El Saeidi, Sonia A., Aglan, Mona S., Temtamy, Samia, AbdelâHamid, Mohame

Journal:

American Journal of Medical Genetics Part A

Year:

2020

File:

PDF, 2.07 MB

2020

2

Comprehensive Assessment of Language Proficiency and Achievement among Learners of English as a Foreign Language

Grant H. Henning, Samira M. Ghawaby, William Zaki Saadalla, Mohamed Ahmed El-Rifai, Ramzy Kamel Hannallah and Mohamed Said Mattar

Journal:

TESOL Quarterly

Year:

1981

File:

PDF, 1.72 MB

1981

3

Further delineation of the clinical spectrum in RNU 4 ATAC related microcephalic osteodysplastic primordial dwarfism type I

Abdel-Salam, Ghada M.H., Abdel-Hamid, Mohamed S., Hassan, Nihal A., Issa, Mahmoud Y., Effat, Laila, Ismail, Samira, Aglan, Mona S., Zaki, Maha S.

Journal:

American Journal of Medical Genetics Part A

Year:

2013

Language:

english

File:

PDF, 1.70 MB

english, 2013

4

Role of vitamin-E on rat liver-amiodarone: An ultrastructural study

Zaki, Mohamed SamirA, Eid, RefaatA

Journal:

Saudi Journal of Gastroenterology

Year:

2009

Language:

english

File:

PDF, 287 KB

english, 2009

5

Molybdenum cofactor and isolated sulphite oxidase deficiencies: Clinical and molecular spectrum among Egyptian patients

Zaki, Maha S., Selim, Laila, EL-Bassyouni, Hala T., Isaa, Mahmoud Y., Mahmoud, Iman, Ismail, Samira, Girgis, Mariane, Sadek, Abdelrahim A., Gleeson, Joseph G., Abdel Hamid, Mohamed S.

Journal:

European Journal of Paediatric Neurology

Year:

2016

Language:

english

File:

PDF, 2.36 MB

english, 2016

6

Megalencephalic leukoencephalopathy with cysts in twelve Egyptian patients: novel mutations inMLC1andHEPACAMand a founder effect

Abdel-Salam, Ghada M. H., Abdel-Hamid, Mohamed S., Ismail, Samira I., Hosny, Heba, Omar, Tarek, Effat, Laila, Aglan, Mona S., Temtamy, Samia A., Zaki, Maha S.

Journal:

Metabolic Brain Disease

Year:

2016

Language:

english

File:

PDF, 4.48 MB

english, 2016

7

Clinical and cytogenetic description of three patients with constitutional mosaic trisomy 8

Ismail, Samira, Kamel, Alaa K., Eid, Maha M., Elruby, Mona O., Aglan, Mona S., Mekkawy, Mona K., Zaki, Maha S., Mohamed, Amal M., Helmy, Nivine A., Temtamy, Samia A.

Journal:

Middle East Journal of Medical Genetics

Year:

2017

Language:

english

File:

PDF, 262 KB

english, 2017

8

GAPO syndrome in seven new patients: Identification of five novel ANTXR1 mutations including the first large intragenic deletion

Abdel-Hamid, Mohamed S., Ismail, Samira, Zaki, Maha S., Abdel-Salam, Ghada M. H., Otaify, Ghada A., Issa, Mahmoud Y., Abdel-Kader, Mohamed, Girgis, Marian, Aboul-Ezz, Eman, Mazen, Inas, Aglan, Mona S.

Journal:

American Journal of Medical Genetics Part A

Year:

2018

Language:

english

File:

PDF, 1.11 MB

english, 2018

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