Subject: Genetics, Medical -- Middle East -- Periodicals - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Subject Genetics, Medical -- Middle East -- Periodicals

1. A case report of FATCO syndrome: fibular aplasia, tibial campomelia, and oligosyndactyly. Issue 1 (January 2015)

Authors:: Bastaki, Laila A.; Al-Hathal, Muneef; Sadik, Doaa I.; Alrohaif, Hadil E.; Yousef, Hala Y.; Khallaf, Mohamed G.
Journal:: Middle East journal of medical genetics
Issue:: Volume 4:Issue 1(2015:Jan.)
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Record Type:: Journal Article
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2. A rare case of isochromosome 10: i(10p) and i(10q). Issue 1 (January 2015)

Authors:: Elbastawisy, Hanan I.; Ghaly, Samuel W.; Abualhasan, Sawsan J.
Journal:: Middle East journal of medical genetics
Issue:: Volume 4:Issue 1(2015:Jan.)
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Record Type:: Journal Article
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3. Abstracts of 13th Asian European workshop on Inborn Errors of Metabolism (AEWIEM) in association with third Human Genetics and Genome Research Division International Conference 18–20 January 2015, Cairo, Egypt. Issue 2 (July 2015)

Authors:: Gouda, Amr
Journal:: Middle East journal of medical genetics
Issue:: Volume 4:Issue 2(2015:Jul.)
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Record Type:: Journal Article
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4. Angiotensin-converting enzyme insertion/deletion polymorphism in an Egyptian cohort of hypertrophic cardiomyopathy. Issue 2 (July 2016)

Authors:: 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.
Journal:: Middle East journal of medical genetics
Issue:: Volume 5:Issue 2(2016:Jul.)
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Record Type:: Journal Article
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5. ARMS2 and HTRA1 gene polymorphisms in association with age-related macular degeneration in an Egyptian cohort. Issue 1 (January 2017)

Authors:: Elhamamsy, May; Souka, Ahmed; El Assi, Hoda H.; Ashraf, Mohammed; Kassem, Heba S.
Journal:: Middle East journal of medical genetics
Issue:: Volume 6:Issue 1(2017:Jan.)
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6. Behavioral problems, biochemical, and anthropometric characteristics of patients with Prader–Willi syndrome. Issue 2 (July 2015)

Authors:: Salah, Ebtissam M.; El-Bassyouni, Hala T.; Kholoussi, Shams; Shehab, Marwa; Kandeel, Wafaa A.
Journal:: Middle East journal of medical genetics
Issue:: Volume 4:Issue 2(2015:Jul.)
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7. Biochemical study of glycogen storage disease type II (Pompe disease) in Egyptian infants. Issue 2 (July 2017)

Authors:: Fateen, Ekram M.; Hamza, Hala S.; Abo-el Matty, Dina M.; Gouda, Amr S.; El-Saiedi, Sonia A.; Saleh, Samy M.; Sobhy Elfeel, Nesrine M.; Youssef Ismail, Mai A.
Journal:: Middle East journal of medical genetics
Issue:: Volume 6:Issue 2(2017:Jul.)
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Record Type:: Journal Article
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8. Cell organelles and inherited metabolic diseases. Issue 1 (January 2016)

Authors:: Gouda, Amr S.
Journal:: Middle East journal of medical genetics
Issue:: Volume 5:Issue 1(2016:Jan.)
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Record Type:: Journal Article
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9. Chromosome 17q duplication associated with 21q telomeric deletion in a female patient with multiple congenital anomalies. Issue 2 (July 2016)

Authors:: Mekkawy, Mona K.; Mazen, Inas M.; Kamel, Alaa K.; Mahmoud, Wael; Mohamed, Amal M.
Journal:: Middle East journal of medical genetics
Issue:: Volume 5:Issue 2(2016:Jul.)
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Record Type:: Journal Article
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10. Clinical and cytogenetic description of three patients with constitutional mosaic trisomy 8. Issue 1 (January 2017)

Authors:: 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
Issue:: Volume 6:Issue 1(2017:Jan.)
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Record Type:: Journal Article
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