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July 2016 - Volume 5 - Issue 2 - Contributor Index

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Abdel Raouf, Haiam

Evaluation of telomerase activity in lymphoproliferative disorders

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Abdelghany, Besra S.

Angiotensin-converting enzyme insertion/deletion polymorphism in an Egyptian cohort of hypertrophic cardiomyopathy

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Abulhasan, Sawsan J.

Pallister–Killian syndrome with fibular hypoplasia: a novel clinical manifestation

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Al-Hathal, Muneef

Pallister–Killian syndrome with fibular hypoplasia: a novel clinical manifestation

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Algendy, Sherif A.

Angiotensin-converting enzyme insertion/deletion polymorphism in an Egyptian cohort of hypertrophic cardiomyopathy

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Ayad, Maha S.

Angiotensin-converting enzyme insertion/deletion polymorphism in an Egyptian cohort of hypertrophic cardiomyopathy

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Azer, Remon S.

Angiotensin-converting enzyme insertion/deletion polymorphism in an Egyptian cohort of hypertrophic cardiomyopathy

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Bastaki, Laila A.

Pallister–Killian syndrome with fibular hypoplasia: a novel clinical manifestation

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Elguindy, Ahmed

Angiotensin-converting enzyme insertion/deletion polymorphism in an Egyptian cohort of hypertrophic cardiomyopathy

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Essawi, Mona L.

Genetic diagnosis of Prader–Willi syndrome

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Ghareeb, Tarek M.

Pallister–Killian syndrome with fibular hypoplasia: a novel clinical manifestation

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Hassan, Heba A.

Genetic diagnosis of Prader–Willi syndrome

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Ismail, Somai

Evaluation of telomerase activity in lymphoproliferative disorders

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Ismail, Suzan R.

Genetic diagnosis of Prader–Willi syndrome

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Kamel, Alaa K.

Chromosome 17q duplication associated with 21q telomeric deletion in a female patient with multiple congenital anomalies

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Kandil, Raina

Evaluation of telomerase activity in lymphoproliferative disorders

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Kassem, Heba Sh.

Angiotensin-converting enzyme insertion/deletion polymorphism in an Egyptian cohort of hypertrophic cardiomyopathy

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Kh, Amr

Evaluation of telomerase activity in lymphoproliferative disorders

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Khedr, Azzah A.

Genetic diagnosis of Prader–Willi syndrome

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Kholoussi, Naglaa M.

Evaluation of telomerase activity in lymphoproliferative disorders

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Magdy, Gehan

Angiotensin-converting enzyme insertion/deletion polymorphism in an Egyptian cohort of hypertrophic cardiomyopathy

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Mahmoud, Wael

Chromosome 17q duplication associated with 21q telomeric deletion in a female patient with multiple congenital anomalies

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Maksoud, Sohier A.

Evaluation of telomerase activity in lymphoproliferative disorders

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Mansour, Osman M.

Evaluation of telomerase activity in lymphoproliferative disorders

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Mazen, Inas M.

Chromosome 17q duplication associated with 21q telomeric deletion in a female patient with multiple congenital anomalies

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Meguid, Nagwa A.

Genetic diagnosis of Prader–Willi syndrome

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Mekkawy, Mona K.

Chromosome 17q duplication associated with 21q telomeric deletion in a female patient with multiple congenital anomalies

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Mohamed, Amal M.

Genetic diagnosis of Prader–Willi syndrome

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Chromosome 17q duplication associated with 21q telomeric deletion in a female patient with multiple congenital anomalies

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Moharem-Elgamal, Sarah

Angiotensin-converting enzyme insertion/deletion polymorphism in an Egyptian cohort of hypertrophic cardiomyopathy

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Nazmy, Nahla A.

Genetic diagnosis of Prader–Willi syndrome

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Razik, Heba A.

Evaluation of telomerase activity in lymphoproliferative disorders

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Sadik, Doaa I.

Pallister–Killian syndrome with fibular hypoplasia: a novel clinical manifestation

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Yacoub, Magdi H.

Angiotensin-converting enzyme insertion/deletion polymorphism in an Egyptian cohort of hypertrophic cardiomyopathy

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Zayed, Shahera A.

Evaluation of telomerase activity in lymphoproliferative disorders

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