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Inas Mazen

Showing results (11-20 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|January 11, 2018
WT1 Gene Mutation, p.R462W, in a 46,XY DSD Patient from Egypt with Gonadoblastoma and Review of the LiteratureInas Mazen, Heba Hassan, Alaa Kamel, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|May 27, 2014
Hereditary 1,25-dihydroxyvitamin D-resistant rickets with alopecia in four Egyptian families: report of three novel mutations in the vitamin D receptor geneInas Mazen, Samira Ismail, Khalda Amr, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|December 23, 2011
AMH gene mutations in two Egyptian families with persistent müllerian duct syndromeInas Mazen, M S Abdel Hamid, M El-Gammal, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|February 1, 2017
Novel AMH and AMHR2 Mutations in Two Egyptian Families with Persistent Müllerian Duct SyndromeInas Mazen, Mona El-Gammal, Ken McElreavey, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|January 12, 2018
Aromatase Deficiency due to a Homozygous CYP19A1 Mutation in a 46,XX Egyptian Patient with Ambiguous GenitaliaInas Mazen, Ken McElreavey, Aya Elaidy, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|January 19, 2022
A Homozygous Missense Variant in Hedgehog Acyltransferase (HHAT) Gene Associated with 46,XY Gonadal DysgenesisInas Mazen, Alaa Kamel, Kenneth McElreavey, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|April 8, 2016
Homozygous Mutation of the FGFR1 Gene Associated with Congenital Heart Disease and 46,XY Disorder of Sex DevelopmentInas Mazen, Heba Amin, Alaa Kamel, et al.
American Journal of Medical Genetics. Part A|March 27, 2019
Biallelic novel missense HHAT variant causes syndromic microcephaly and cerebellar-vermis hypoplasiaGhada M H Abdel-Salam, Inas Mazen, Maha Eid, et al.
Hormones (Athens, Greece)|March 25, 2024
Expanding the phenotypic spectrum of LHCGR signal peptide insertion variant: novel clinical and allelic findings causing Leydig cell hypoplasia type IIHeba Amin Hassan, Inas Mazen, Aya Elaidy, et al.
Hormone Research in Paediatrics|July 19, 2014
A novel mutation (c.2735_2736delTC) in the androgen receptor gene in 46,XY females with complete androgen insensitivity syndrome in an Egyptian familyInas Mazen, Hala Soliman, Mona El-Gammal, et al.
Pageof 5

Showing results (11-20 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|January 11, 2018
WT1 Gene Mutation, p.R462W, in a 46,XY DSD Patient from Egypt with Gonadoblastoma and Review of the LiteratureInas Mazen, Heba Hassan, Alaa Kamel, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|May 27, 2014
Hereditary 1,25-dihydroxyvitamin D-resistant rickets with alopecia in four Egyptian families: report of three novel mutations in the vitamin D receptor geneInas Mazen, Samira Ismail, Khalda Amr, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|December 23, 2011
AMH gene mutations in two Egyptian families with persistent müllerian duct syndromeInas Mazen, M S Abdel Hamid, M El-Gammal, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|February 1, 2017
Novel AMH and AMHR2 Mutations in Two Egyptian Families with Persistent Müllerian Duct SyndromeInas Mazen, Mona El-Gammal, Ken McElreavey, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|January 12, 2018
Aromatase Deficiency due to a Homozygous CYP19A1 Mutation in a 46,XX Egyptian Patient with Ambiguous GenitaliaInas Mazen, Ken McElreavey, Aya Elaidy, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|January 19, 2022
A Homozygous Missense Variant in Hedgehog Acyltransferase (HHAT) Gene Associated with 46,XY Gonadal DysgenesisInas Mazen, Alaa Kamel, Kenneth McElreavey, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|April 8, 2016
Homozygous Mutation of the FGFR1 Gene Associated with Congenital Heart Disease and 46,XY Disorder of Sex DevelopmentInas Mazen, Heba Amin, Alaa Kamel, et al.
American Journal of Medical Genetics. Part A|March 27, 2019
Biallelic novel missense HHAT variant causes syndromic microcephaly and cerebellar-vermis hypoplasiaGhada M H Abdel-Salam, Inas Mazen, Maha Eid, et al.
Hormones (Athens, Greece)|March 25, 2024
Expanding the phenotypic spectrum of LHCGR signal peptide insertion variant: novel clinical and allelic findings causing Leydig cell hypoplasia type IIHeba Amin Hassan, Inas Mazen, Aya Elaidy, et al.
Hormone Research in Paediatrics|July 19, 2014
A novel mutation (c.2735_2736delTC) in the androgen receptor gene in 46,XY females with complete androgen insensitivity syndrome in an Egyptian familyInas Mazen, Hala Soliman, Mona El-Gammal, et al.
Pageof 5