Evaluation of telomerase activity in lymphoproliferative disorders Zayed, Shahera A.; Mansour, Osman M.; Kholoussi, Naglaa M.; More Zayed, Shahera A.; Mansour, Osman M.; Kholoussi, Naglaa M.; Razik, Heba A.; Kh, Amr; Maksoud, Sohier A.; Abdel Raouf, Haiam; Ismail, Somai; Kandil, Raina Less Middle East Journal of Medical Genetics. 5(2):60-64, July 2016. Abstract Abstract Favorite PDF Permissions Buy
Angiotensin-converting enzyme insertion/deletion polymorphism in an Egyptian cohort of hypertrophic cardiomyopathy Kassem, Heba Sh.; Algendy, Sherif A.; Azer, Remon S.; More 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. Less Middle East Journal of Medical Genetics. 5(2):65-70, July 2016. Abstract Abstract Favorite PDF Permissions Buy
Pallister–Killian syndrome with fibular hypoplasia: a novel clinical manifestation Sadik, Doaa I.; Al-Hathal, Muneef; Ghareeb, Tarek M.; More Sadik, Doaa I.; Al-Hathal, Muneef; Ghareeb, Tarek M.; Abulhasan, Sawsan J.; Bastaki, Laila A. Less Middle East Journal of Medical Genetics. 5(2):41-44, July 2016. Abstract Abstract Favorite PDF Permissions Buy
Pallister–Killian syndrome with fibular hypoplasia: a novel clinical manifestation Sadik, Doaa I.; Al-Hathal, Muneef; Ghareeb, Tarek M.; More Sadik, Doaa I.; Al-Hathal, Muneef; Ghareeb, Tarek M.; Abulhasan, Sawsan J.; Bastaki, Laila A. Less Middle East Journal of Medical Genetics. 5(2):41-44, July 2016. Abstract Abstract Favorite PDF Permissions Buy
Angiotensin-converting enzyme insertion/deletion polymorphism in an Egyptian cohort of hypertrophic cardiomyopathy Kassem, Heba Sh.; Algendy, Sherif A.; Azer, Remon S.; More 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. Less Middle East Journal of Medical Genetics. 5(2):65-70, July 2016. Abstract Abstract Favorite PDF Permissions Buy
Angiotensin-converting enzyme insertion/deletion polymorphism in an Egyptian cohort of hypertrophic cardiomyopathy Kassem, Heba Sh.; Algendy, Sherif A.; Azer, Remon S.; More 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. Less Middle East Journal of Medical Genetics. 5(2):65-70, July 2016. Abstract Abstract Favorite PDF Permissions Buy
Angiotensin-converting enzyme insertion/deletion polymorphism in an Egyptian cohort of hypertrophic cardiomyopathy Kassem, Heba Sh.; Algendy, Sherif A.; Azer, Remon S.; More 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. Less Middle East Journal of Medical Genetics. 5(2):65-70, July 2016. Abstract Abstract Favorite PDF Permissions Buy
Pallister–Killian syndrome with fibular hypoplasia: a novel clinical manifestation Sadik, Doaa I.; Al-Hathal, Muneef; Ghareeb, Tarek M.; More Sadik, Doaa I.; Al-Hathal, Muneef; Ghareeb, Tarek M.; Abulhasan, Sawsan J.; Bastaki, Laila A. Less Middle East Journal of Medical Genetics. 5(2):41-44, July 2016. Abstract Abstract Favorite PDF Permissions Buy
Angiotensin-converting enzyme insertion/deletion polymorphism in an Egyptian cohort of hypertrophic cardiomyopathy Kassem, Heba Sh.; Algendy, Sherif A.; Azer, Remon S.; More 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. Less Middle East Journal of Medical Genetics. 5(2):65-70, July 2016. Abstract Abstract Favorite PDF Permissions Buy
Genetic diagnosis of Prader–Willi syndrome Khedr, Azzah A.; Meguid, Nagwa A.; Mohamed, Amal M.; More Khedr, Azzah A.; Meguid, Nagwa A.; Mohamed, Amal M.; Ismail, Suzan R.; Nazmy, Nahla A.; Hassan, Heba A.; Essawi, Mona L. Less Middle East Journal of Medical Genetics. 5(2):45-53, July 2016. Abstract Abstract Favorite PDF Permissions Buy
Pallister–Killian syndrome with fibular hypoplasia: a novel clinical manifestation Sadik, Doaa I.; Al-Hathal, Muneef; Ghareeb, Tarek M.; More Sadik, Doaa I.; Al-Hathal, Muneef; Ghareeb, Tarek M.; Abulhasan, Sawsan J.; Bastaki, Laila A. Less Middle East Journal of Medical Genetics. 5(2):41-44, July 2016. Abstract Abstract Favorite PDF Permissions Buy
Genetic diagnosis of Prader–Willi syndrome Khedr, Azzah A.; Meguid, Nagwa A.; Mohamed, Amal M.; More Khedr, Azzah A.; Meguid, Nagwa A.; Mohamed, Amal M.; Ismail, Suzan R.; Nazmy, Nahla A.; Hassan, Heba A.; Essawi, Mona L. Less Middle East Journal of Medical Genetics. 5(2):45-53, July 2016. Abstract Abstract Favorite PDF Permissions Buy
Evaluation of telomerase activity in lymphoproliferative disorders Zayed, Shahera A.; Mansour, Osman M.; Kholoussi, Naglaa M.; More Zayed, Shahera A.; Mansour, Osman M.; Kholoussi, Naglaa M.; Razik, Heba A.; Kh, Amr; Maksoud, Sohier A.; Abdel Raouf, Haiam; Ismail, Somai; Kandil, Raina Less Middle East Journal of Medical Genetics. 5(2):60-64, July 2016. Abstract Abstract Favorite PDF Permissions Buy
Genetic diagnosis of Prader–Willi syndrome Khedr, Azzah A.; Meguid, Nagwa A.; Mohamed, Amal M.; More Khedr, Azzah A.; Meguid, Nagwa A.; Mohamed, Amal M.; Ismail, Suzan R.; Nazmy, Nahla A.; Hassan, Heba A.; Essawi, Mona L. Less Middle East Journal of Medical Genetics. 5(2):45-53, July 2016. Abstract Abstract Favorite PDF Permissions Buy
Chromosome 17q duplication associated with 21q telomeric deletion in a female patient with multiple congenital anomalies Mekkawy, Mona K.; Mazen, Inas M.; Kamel, Alaa K.; More Mekkawy, Mona K.; Mazen, Inas M.; Kamel, Alaa K.; Mahmoud, Wael; Mohamed, Amal M. Less Middle East Journal of Medical Genetics. 5(2):54-59, July 2016. Abstract Abstract Favorite PDF Permissions Buy
Evaluation of telomerase activity in lymphoproliferative disorders Zayed, Shahera A.; Mansour, Osman M.; Kholoussi, Naglaa M.; More Zayed, Shahera A.; Mansour, Osman M.; Kholoussi, Naglaa M.; Razik, Heba A.; Kh, Amr; Maksoud, Sohier A.; Abdel Raouf, Haiam; Ismail, Somai; Kandil, Raina Less Middle East Journal of Medical Genetics. 5(2):60-64, July 2016. Abstract Abstract Favorite PDF Permissions Buy
Angiotensin-converting enzyme insertion/deletion polymorphism in an Egyptian cohort of hypertrophic cardiomyopathy Kassem, Heba Sh.; Algendy, Sherif A.; Azer, Remon S.; More 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. Less Middle East Journal of Medical Genetics. 5(2):65-70, July 2016. Abstract Abstract Favorite PDF Permissions Buy
Evaluation of telomerase activity in lymphoproliferative disorders Zayed, Shahera A.; Mansour, Osman M.; Kholoussi, Naglaa M.; More Zayed, Shahera A.; Mansour, Osman M.; Kholoussi, Naglaa M.; Razik, Heba A.; Kh, Amr; Maksoud, Sohier A.; Abdel Raouf, Haiam; Ismail, Somai; Kandil, Raina Less Middle East Journal of Medical Genetics. 5(2):60-64, July 2016. Abstract Abstract Favorite PDF Permissions Buy
Genetic diagnosis of Prader–Willi syndrome Khedr, Azzah A.; Meguid, Nagwa A.; Mohamed, Amal M.; More Khedr, Azzah A.; Meguid, Nagwa A.; Mohamed, Amal M.; Ismail, Suzan R.; Nazmy, Nahla A.; Hassan, Heba A.; Essawi, Mona L. Less Middle East Journal of Medical Genetics. 5(2):45-53, July 2016. Abstract Abstract Favorite PDF Permissions Buy
Evaluation of telomerase activity in lymphoproliferative disorders Zayed, Shahera A.; Mansour, Osman M.; Kholoussi, Naglaa M.; More Zayed, Shahera A.; Mansour, Osman M.; Kholoussi, Naglaa M.; Razik, Heba A.; Kh, Amr; Maksoud, Sohier A.; Abdel Raouf, Haiam; Ismail, Somai; Kandil, Raina Less Middle East Journal of Medical Genetics. 5(2):60-64, July 2016. Abstract Abstract Favorite PDF Permissions Buy
Angiotensin-converting enzyme insertion/deletion polymorphism in an Egyptian cohort of hypertrophic cardiomyopathy Kassem, Heba Sh.; Algendy, Sherif A.; Azer, Remon S.; More 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. Less Middle East Journal of Medical Genetics. 5(2):65-70, July 2016. Abstract Abstract Favorite PDF Permissions Buy
Chromosome 17q duplication associated with 21q telomeric deletion in a female patient with multiple congenital anomalies Mekkawy, Mona K.; Mazen, Inas M.; Kamel, Alaa K.; More Mekkawy, Mona K.; Mazen, Inas M.; Kamel, Alaa K.; Mahmoud, Wael; Mohamed, Amal M. Less Middle East Journal of Medical Genetics. 5(2):54-59, July 2016. Abstract Abstract Favorite PDF Permissions Buy
Evaluation of telomerase activity in lymphoproliferative disorders Zayed, Shahera A.; Mansour, Osman M.; Kholoussi, Naglaa M.; More Zayed, Shahera A.; Mansour, Osman M.; Kholoussi, Naglaa M.; Razik, Heba A.; Kh, Amr; Maksoud, Sohier A.; Abdel Raouf, Haiam; Ismail, Somai; Kandil, Raina Less Middle East Journal of Medical Genetics. 5(2):60-64, July 2016. Abstract Abstract Favorite PDF Permissions Buy
Evaluation of telomerase activity in lymphoproliferative disorders Zayed, Shahera A.; Mansour, Osman M.; Kholoussi, Naglaa M.; More Zayed, Shahera A.; Mansour, Osman M.; Kholoussi, Naglaa M.; Razik, Heba A.; Kh, Amr; Maksoud, Sohier A.; Abdel Raouf, Haiam; Ismail, Somai; Kandil, Raina Less Middle East Journal of Medical Genetics. 5(2):60-64, July 2016. Abstract Abstract Favorite PDF Permissions Buy
Chromosome 17q duplication associated with 21q telomeric deletion in a female patient with multiple congenital anomalies Mekkawy, Mona K.; Mazen, Inas M.; Kamel, Alaa K.; More Mekkawy, Mona K.; Mazen, Inas M.; Kamel, Alaa K.; Mahmoud, Wael; Mohamed, Amal M. Less Middle East Journal of Medical Genetics. 5(2):54-59, July 2016. Abstract Abstract Favorite PDF Permissions Buy
Genetic diagnosis of Prader–Willi syndrome Khedr, Azzah A.; Meguid, Nagwa A.; Mohamed, Amal M.; More Khedr, Azzah A.; Meguid, Nagwa A.; Mohamed, Amal M.; Ismail, Suzan R.; Nazmy, Nahla A.; Hassan, Heba A.; Essawi, Mona L. Less Middle East Journal of Medical Genetics. 5(2):45-53, July 2016. Abstract Abstract Favorite PDF Permissions Buy
Chromosome 17q duplication associated with 21q telomeric deletion in a female patient with multiple congenital anomalies Mekkawy, Mona K.; Mazen, Inas M.; Kamel, Alaa K.; More Mekkawy, Mona K.; Mazen, Inas M.; Kamel, Alaa K.; Mahmoud, Wael; Mohamed, Amal M. Less Middle East Journal of Medical Genetics. 5(2):54-59, July 2016. Abstract Abstract Favorite PDF Permissions Buy
Genetic diagnosis of Prader–Willi syndrome Khedr, Azzah A.; Meguid, Nagwa A.; Mohamed, Amal M.; More Khedr, Azzah A.; Meguid, Nagwa A.; Mohamed, Amal M.; Ismail, Suzan R.; Nazmy, Nahla A.; Hassan, Heba A.; Essawi, Mona L. Less Middle East Journal of Medical Genetics. 5(2):45-53, July 2016. Abstract Abstract Favorite PDF Permissions Buy
Chromosome 17q duplication associated with 21q telomeric deletion in a female patient with multiple congenital anomalies Mekkawy, Mona K.; Mazen, Inas M.; Kamel, Alaa K.; More Mekkawy, Mona K.; Mazen, Inas M.; Kamel, Alaa K.; Mahmoud, Wael; Mohamed, Amal M. Less Middle East Journal of Medical Genetics. 5(2):54-59, July 2016. Abstract Abstract Favorite PDF Permissions Buy
Angiotensin-converting enzyme insertion/deletion polymorphism in an Egyptian cohort of hypertrophic cardiomyopathy Kassem, Heba Sh.; Algendy, Sherif A.; Azer, Remon S.; More 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. Less Middle East Journal of Medical Genetics. 5(2):65-70, July 2016. Abstract Abstract Favorite PDF Permissions Buy
Genetic diagnosis of Prader–Willi syndrome Khedr, Azzah A.; Meguid, Nagwa A.; Mohamed, Amal M.; More Khedr, Azzah A.; Meguid, Nagwa A.; Mohamed, Amal M.; Ismail, Suzan R.; Nazmy, Nahla A.; Hassan, Heba A.; Essawi, Mona L. Less Middle East Journal of Medical Genetics. 5(2):45-53, July 2016. Abstract Abstract Favorite PDF Permissions Buy
Evaluation of telomerase activity in lymphoproliferative disorders Zayed, Shahera A.; Mansour, Osman M.; Kholoussi, Naglaa M.; More Zayed, Shahera A.; Mansour, Osman M.; Kholoussi, Naglaa M.; Razik, Heba A.; Kh, Amr; Maksoud, Sohier A.; Abdel Raouf, Haiam; Ismail, Somai; Kandil, Raina Less Middle East Journal of Medical Genetics. 5(2):60-64, July 2016. Abstract Abstract Favorite PDF Permissions Buy
Pallister–Killian syndrome with fibular hypoplasia: a novel clinical manifestation Sadik, Doaa I.; Al-Hathal, Muneef; Ghareeb, Tarek M.; More Sadik, Doaa I.; Al-Hathal, Muneef; Ghareeb, Tarek M.; Abulhasan, Sawsan J.; Bastaki, Laila A. Less Middle East Journal of Medical Genetics. 5(2):41-44, July 2016. Abstract Abstract Favorite PDF Permissions Buy
Angiotensin-converting enzyme insertion/deletion polymorphism in an Egyptian cohort of hypertrophic cardiomyopathy Kassem, Heba Sh.; Algendy, Sherif A.; Azer, Remon S.; More 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. Less Middle East Journal of Medical Genetics. 5(2):65-70, July 2016. Abstract Abstract Favorite PDF Permissions Buy
Evaluation of telomerase activity in lymphoproliferative disorders Zayed, Shahera A.; Mansour, Osman M.; Kholoussi, Naglaa M.; More Zayed, Shahera A.; Mansour, Osman M.; Kholoussi, Naglaa M.; Razik, Heba A.; Kh, Amr; Maksoud, Sohier A.; Abdel Raouf, Haiam; Ismail, Somai; Kandil, Raina Less Middle East Journal of Medical Genetics. 5(2):60-64, July 2016. Abstract Abstract Favorite PDF Permissions Buy
