Scientific Programme, ePosters & Abstracts
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Novel Heterozygous Mutation in Wilms Tumor 1 Gene in Patient with Mixed Gonadal Dysgenesis | ESPE2019 Heba Hassan; Mona Essawi; Mona Mekkawy; Alaa Kamel; Inas Mazen http://abstracts.eurospe.org/hrp/0092/hrp0092P3-230 Published: 2019-08-22
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A Clinical and Cytogenetic Study of Patients with Disorders of Sex Development (DSDs) Associated with Congenital Anomalies or Recognizable Syndromes | ESPE2019 Inas Mazen; Mona Mekkawi; Alaa Kamel; Sherif Waly; Abeer Atef; Ahmed Torky; Gammal Mona El http://abstracts.eurospe.org/hrp/0092/hrp0092P2-256 Published: 2019-08-22
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Mutations in the DEAH-box RNA Helicase DHX37 are a Frequent Cause of 46,XY Gonadal Dysgenesis and 46,XY Testicular Regression Syndrome | ESPE2019 Ken McElreavey; Anne Jorgensen; Caroline Eozenou; Tiphanie Merel; Joelle Bignon-Topalovic; Daisy Tan; Denis Houzelstein; Federic http://abstracts.eurospe.org/hrp/0092/hrp0092FC10.3 Published: 2019-08-22
Novel Heterozygous Mutation in Wilms Tumor 1 Gene in Patient with Mixed Gonadal Dysgenesis | ESPE2019 Heba Hassan; Mona Essawi; Mona Mekkawy; Alaa Kamel; Inas Mazen http://abstracts.eurospe.org/hrp/0092/hrp0092p3-230.html Published: 2019-08-22
A Clinical and Cytogenetic Study of Patients with Disorders of Sex Development (DSDs) Associated with Congenital Anomalies or Recognizable Syndromes | ESPE2019 Inas Mazen; Mona Mekkawi; Alaa Kamel; Sherif Waly; Abeer Atef; Ahmed Torky; Gammal Mona El http://abstracts.eurospe.org/hrp/0092/hrp0092p2-256.html Published: 2019-08-22
Mutations in the DEAH-box RNA Helicase DHX37 are a Frequent Cause of 46,XY Gonadal Dysgenesis and 46,XY Testicular Regression Syndrome | ESPE2019 Ken McElreavey; Anne Jorgensen; Caroline Eozenou; Tiphanie Merel; Joelle Bignon-Topalovic; Daisy Tan; Denis Houzelstein; Federic http://abstracts.eurospe.org/hrp/0092/hrp0092fc10.3.html Published: 2019-08-22
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Cytogenetic Spectrum of Ovotesticular Disorder of Sex Development in Egyptian DSD Patients | ESPE2018 Inas Mazen; Mona Mekkawi; Nabil Dessouki; Amal Mohammed; Alaa Kamel http://abstracts.eurospe.org/hrp/0089/hrp0089p3-p341.htm Published: 2018-08-28
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Cytogenetic Spectrum of Ovotesticular Disorder of Sex Development in Egyptian DSD Patients | ESPE2018 Inas Mazen; Mona Mekkawi; Nabil Dessouki http://abstracts.eurospe.org/hrp/0089/hrp0089p3-p340.htm Published: 2018-08-28
Novel AMH and AMHR-II Mutations in Two Egyptian Families with Persistent Mullerian Duct Syndrome | ESPE2016 Inas Mazen; Gammal Mona El; Aidy Aya El; Hamid Mohamed Abdel http://abstracts.eurospe.org/hrp/0086/hrp0086p2-p429.htm Published: 2016-08-19
Cytogenetic Study of Sex Chromosomal Abnormalities in Egyptian DSD Patients | ESPE2016 Inas Mazen; Alaa Kamel; Mona Mekkawi; aidy Aya El http://abstracts.eurospe.org/hrp/0086/hrp0086p2-p417.htm Published: 2016-08-19
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