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Anu Bashamboo

Showing results (31-40 of 94) with videos related to

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Reproductive Biomedicine Online|March 2, 2012
Polymorphisms in DLGH1 and LAMC1 in Mayer-Rokitansky-Kuster-Hauser syndromeCelia Ravel, Anu Bashamboo, Joelle Bignon-Topalovic, et al.
Fertility and Sterility|February 4, 2014
Prevalence of the Aurora kinase C c.144delC mutation in infertile Moroccan menAbdelmajid Eloualid, Hassan Rouba, Houria Rhaissi, 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.
Fertility and Sterility|August 7, 2013
Methylation changes in mature sperm deoxyribonucleic acid from oligozoospermic men: assessment of genetic variants and assisted reproductive technology outcomeDebbie Montjean, Célia Ravel, Moncef Benkhalifa, et al.
Andrologia|April 10, 2020
A missense mutation in NR5A1 causing female to male sex reversal: A case reportMasomeh Askari, Mandana Rastari, Mehrshad Seresht-Ahmadi, et al.
Journal of Cell Science|July 6, 2006
The survival of differentiating embryonic stem cells is dependent on the SCF-KIT pathwayAnu Bashamboo, A Helen Taylor, Kay Samuel, 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.
BMC Pediatrics|December 1, 2016
Familial forms of disorders of sex development may be common if infertility is considered a comorbidityRaja Brauner, Flavia Picard-Dieval, Henri Lottmann, et al.
Plos One|November 9, 2013
Congenital hypogonadotropic hypogonadism during childhood: presentation and genetic analyses in 46 boysAudrey Vizeneux, Aude Hilfiger, Jérôme Bouligand, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|January 20, 2025
Clinical and genetic diagnosis of first cohort of differences of sexual development in the Iranian populationMandana Rastari, Masomeh Askari, Kenneth McElreavey, et al.
Pageof 10

Showing results (31-40 of 94) with videos related to

Sort By:
Pageof 10
Reproductive Biomedicine Online|March 2, 2012
Polymorphisms in DLGH1 and LAMC1 in Mayer-Rokitansky-Kuster-Hauser syndromeCelia Ravel, Anu Bashamboo, Joelle Bignon-Topalovic, et al.
Fertility and Sterility|February 4, 2014
Prevalence of the Aurora kinase C c.144delC mutation in infertile Moroccan menAbdelmajid Eloualid, Hassan Rouba, Houria Rhaissi, 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.
Fertility and Sterility|August 7, 2013
Methylation changes in mature sperm deoxyribonucleic acid from oligozoospermic men: assessment of genetic variants and assisted reproductive technology outcomeDebbie Montjean, Célia Ravel, Moncef Benkhalifa, et al.
Andrologia|April 10, 2020
A missense mutation in NR5A1 causing female to male sex reversal: A case reportMasomeh Askari, Mandana Rastari, Mehrshad Seresht-Ahmadi, et al.
Journal of Cell Science|July 6, 2006
The survival of differentiating embryonic stem cells is dependent on the SCF-KIT pathwayAnu Bashamboo, A Helen Taylor, Kay Samuel, 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.
BMC Pediatrics|December 1, 2016
Familial forms of disorders of sex development may be common if infertility is considered a comorbidityRaja Brauner, Flavia Picard-Dieval, Henri Lottmann, et al.
Plos One|November 9, 2013
Congenital hypogonadotropic hypogonadism during childhood: presentation and genetic analyses in 46 boysAudrey Vizeneux, Aude Hilfiger, Jérôme Bouligand, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|January 20, 2025
Clinical and genetic diagnosis of first cohort of differences of sexual development in the Iranian populationMandana Rastari, Masomeh Askari, Kenneth McElreavey, et al.
Pageof 10