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Inas Mazen

Showing results (21-30 of 49) with videos related to

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Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|April 14, 2016
Mutational Profile of 10 Afflicted Egyptian Families with 17-β-HSD-3 DeficiencyHeba Amin Hassan, Inas Mazen, Yehia Zakaria Gad, et al.
Reproductive Biology|March 3, 2020
Detection of low-grade mosaicism and its correlation with hormonal profile, testicular volume, and semen quality in a cohort of Egyptian Klinefelter and Klinefelter-like patientsAbdelrahman Madian, Maha M Eid, Adel A B Shahin, et al.
Cytogenetic and Genome Research|October 2, 2018
Unbalanced 14;X Translocation and Pattern of X Inactivation in a Female Patient with Multiple Congenital AnomaliesAmal Mahmoud Mohamed, Maha S Zaki, Alaa K Kamel, et al.
Journal, Genetic Engineering & Biotechnology|July 29, 2021
IGF1R, IGFALS, and IGFBP3 gene copy number variations in a group of non-syndromic Egyptian short childrenIslam M Fadel, Moustafa H Ragab, Ola M Eid, et al.
American Journal of Medical Genetics. Part A|May 26, 2012
Isodicentric Y chromosomes in Egyptian patients with disorders of sex development (DSD)Mona Mekkawy, Alaa Kamel, Mona El-Ruby, et al.
European Journal of Endocrinology|May 15, 2009
The spectrum of phenotypes associated with mutations in steroidogenic factor 1 (SF-1, NR5A1, Ad4BP) includes severe penoscrotal hypospadias in 46,XY males without adrenal insufficiencyBirgit Köhler, Lin Lin, Inas Mazen, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|May 13, 2016
Identification of NR5A1 Mutations and Possible Digenic Inheritance in 46,XY Gonadal DysgenesisInas Mazen, Mohamed Abdel-Hamid, Mona Mekkawy, et al.
The Journal of Sexual Medicine|September 2, 2017
Biochemical Analysis of Four Missense Mutations in the HSD17B3 Gene Associated With 46,XY Disorders of Sex Development in Egyptian PatientsRoger T Engeli, Maria Tsachaki, Heba A Hassan, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|July 3, 2020
Assessment of the most common CYP21A2 point mutations in a cohort of congenital adrenal hyperplasia patients from EgyptMona Essawi, Inas Mazen, Lubna Fawaz, et al.
American Journal of Medical Genetics. Part A|March 20, 2021
Advances in genomic diagnosis of a large cohort of Egyptian patients with disorders of sex developmentInas Mazen, Mona Mekkawy, Alaa Kamel, et al.
Pageof 5

Showing results (21-30 of 49) with videos related to

Sort By:
Pageof 5
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|April 14, 2016
Mutational Profile of 10 Afflicted Egyptian Families with 17-β-HSD-3 DeficiencyHeba Amin Hassan, Inas Mazen, Yehia Zakaria Gad, et al.
Reproductive Biology|March 3, 2020
Detection of low-grade mosaicism and its correlation with hormonal profile, testicular volume, and semen quality in a cohort of Egyptian Klinefelter and Klinefelter-like patientsAbdelrahman Madian, Maha M Eid, Adel A B Shahin, et al.
Cytogenetic and Genome Research|October 2, 2018
Unbalanced 14;X Translocation and Pattern of X Inactivation in a Female Patient with Multiple Congenital AnomaliesAmal Mahmoud Mohamed, Maha S Zaki, Alaa K Kamel, et al.
Journal, Genetic Engineering & Biotechnology|July 29, 2021
IGF1R, IGFALS, and IGFBP3 gene copy number variations in a group of non-syndromic Egyptian short childrenIslam M Fadel, Moustafa H Ragab, Ola M Eid, et al.
American Journal of Medical Genetics. Part A|May 26, 2012
Isodicentric Y chromosomes in Egyptian patients with disorders of sex development (DSD)Mona Mekkawy, Alaa Kamel, Mona El-Ruby, et al.
European Journal of Endocrinology|May 15, 2009
The spectrum of phenotypes associated with mutations in steroidogenic factor 1 (SF-1, NR5A1, Ad4BP) includes severe penoscrotal hypospadias in 46,XY males without adrenal insufficiencyBirgit Köhler, Lin Lin, Inas Mazen, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|May 13, 2016
Identification of NR5A1 Mutations and Possible Digenic Inheritance in 46,XY Gonadal DysgenesisInas Mazen, Mohamed Abdel-Hamid, Mona Mekkawy, et al.
The Journal of Sexual Medicine|September 2, 2017
Biochemical Analysis of Four Missense Mutations in the HSD17B3 Gene Associated With 46,XY Disorders of Sex Development in Egyptian PatientsRoger T Engeli, Maria Tsachaki, Heba A Hassan, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|July 3, 2020
Assessment of the most common CYP21A2 point mutations in a cohort of congenital adrenal hyperplasia patients from EgyptMona Essawi, Inas Mazen, Lubna Fawaz, et al.
American Journal of Medical Genetics. Part A|March 20, 2021
Advances in genomic diagnosis of a large cohort of Egyptian patients with disorders of sex developmentInas Mazen, Mona Mekkawy, Alaa Kamel, et al.
Pageof 5