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Inas Mazen

Showing results (1-10 of 49) with videos related to

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Endocrine Development|September 24, 2014
Achieving diagnostic certainty in resource-limited settingsJamal Raza, Inas Mazen
American Journal of Medical Genetics. Part A|October 15, 2011
Tissue-specific mosaicism for tetrasomy 9p uncovered by array CGHMarwa I Shehab, Inas Mazen, Susan Bint
Clinical Dysmorphology|January 7, 2003
Transposition of external genitalia and associated malformationsNagwa Abdel Meguid, Samia A Temtamy, Inas Mazen
Journal of Pediatric Endocrinology & Metabolism : JPEM|December 17, 2010
Variable associations of Klinefelter syndrome in childrenInas Mazen, Mona El-Ruby, Hala T El-Bassyouni
Journal of Pediatric Endocrinology & Metabolism : JPEM|April 26, 2003
A novel mutation of the 5alpha-reductase type 2 gene in two unrelated Egyptian children with ambiguous genitaliaInas Mazen, Mona Hafez, Mona Mamdouh, et al.
Hormone Research|June 5, 2003
A new mutation of 5-alpha-reductase type 2 (A62E) in a large Egyptian kindredMona Hafez, Inas Mazen, Isis Ghali, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|July 23, 2018
A Homozygous Missense Mutation in FANCA Gene in a 46,XY Female with Gonadal DysgenesisInas Mazen, Kenneth McElreavey, Maha M Eid, et al.
Clinical Endocrinology|April 18, 2003
Molecular analysis of 5alpha-reductase type 2 gene in eight unrelated egyptian children with suspected 5alpha-reductase deficiency: prevalence of the G34R mutationInas Mazen, Yehia Z Gad, Mona Hafez, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|June 15, 2020
Cytogenetic Spectrum of Ovotesticular Difference of Sex Development (OT DSD) among a Large Cohort of DSD Patients and Literature ReviewMona K Mekkawy, Alaa K Kamel, Nabil Dessouky, et al.
Molecular Genetics and Metabolism Reports|November 30, 2016
A novel mutation in the leptin gene (W121X) in an Egyptian familyInas Mazen, Khalda Amr, Sally Tantawy, et al.
Pageof 5

Showing results (1-10 of 49) with videos related to

Sort By:
Pageof 5
Endocrine Development|September 24, 2014
Achieving diagnostic certainty in resource-limited settingsJamal Raza, Inas Mazen
American Journal of Medical Genetics. Part A|October 15, 2011
Tissue-specific mosaicism for tetrasomy 9p uncovered by array CGHMarwa I Shehab, Inas Mazen, Susan Bint
Clinical Dysmorphology|January 7, 2003
Transposition of external genitalia and associated malformationsNagwa Abdel Meguid, Samia A Temtamy, Inas Mazen
Journal of Pediatric Endocrinology & Metabolism : JPEM|December 17, 2010
Variable associations of Klinefelter syndrome in childrenInas Mazen, Mona El-Ruby, Hala T El-Bassyouni
Journal of Pediatric Endocrinology & Metabolism : JPEM|April 26, 2003
A novel mutation of the 5alpha-reductase type 2 gene in two unrelated Egyptian children with ambiguous genitaliaInas Mazen, Mona Hafez, Mona Mamdouh, et al.
Hormone Research|June 5, 2003
A new mutation of 5-alpha-reductase type 2 (A62E) in a large Egyptian kindredMona Hafez, Inas Mazen, Isis Ghali, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|July 23, 2018
A Homozygous Missense Mutation in FANCA Gene in a 46,XY Female with Gonadal DysgenesisInas Mazen, Kenneth McElreavey, Maha M Eid, et al.
Clinical Endocrinology|April 18, 2003
Molecular analysis of 5alpha-reductase type 2 gene in eight unrelated egyptian children with suspected 5alpha-reductase deficiency: prevalence of the G34R mutationInas Mazen, Yehia Z Gad, Mona Hafez, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|June 15, 2020
Cytogenetic Spectrum of Ovotesticular Difference of Sex Development (OT DSD) among a Large Cohort of DSD Patients and Literature ReviewMona K Mekkawy, Alaa K Kamel, Nabil Dessouky, et al.
Molecular Genetics and Metabolism Reports|November 30, 2016
A novel mutation in the leptin gene (W121X) in an Egyptian familyInas Mazen, Khalda Amr, Sally Tantawy, et al.
Pageof 5