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Anu Bashamboo

Showing results (41-50 of 94) with videos related to

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Fertility and Sterility|May 26, 2009
Mutations in the TSPYL1 gene associated with 46,XY disorder of sex development and male infertilityGiovanna Vinci, Raja Brauner, Attila Tar, et al.
Human Molecular Genetics|February 20, 2014
Mutations in the FOG2/ZFPM2 gene are associated with anomalies of human testis determinationAnu Bashamboo, Raja Brauner, Joelle Bignon-Topalovic, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|July 31, 2014
A child with a novel de novo mutation in the aristaless domain of the aristaless-related homeobox (ARX) gene presenting with ambiguous genitalia and psychomotor delayNirmala Dushyanthi Sirisena, Kenneth McElreavey, Anu Bashamboo, et al.
Human Mutation|October 19, 2012
Unilateral cryptorchidism in mice mutant for PtgdsPascal Philibert, Brigitte Boizet-Bonhoure, Anu Bashamboo, et al.
Fertility and Sterility|October 5, 2010
Polymorphisms in MTHFR and MTRR genes associated with blood plasma homocysteine concentration and sperm countsDebbie Montjean, Moncef Benkhalifa, Lionel Dessolle, et al.
Gene|December 21, 2025
A novel candidate missense variant in the catalytic domain of USP26 associated with asthenoteratozoospermiaSeyedeh Zahra Mousavi, Masomeh Askari, Ken McElreavey, et al.
Fertility and Sterility|March 28, 2015
Genetic mutations and somatic anomalies in association with 46,XY gonadal dysgenesisClaire Bastian, Jean-Baptiste Muller, Stephen Lortat-Jacob, 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.
Plos One|July 2, 2010
Clinical, biological and genetic analysis of prepubertal isolated ovarian cyst in 11 girlsRaja Brauner, Anu Bashamboo, Sébastien Rouget, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|December 21, 2017
A Novel Homozygous Missense Mutation in the FU-CRD2 Domain of the R-spondin1 Gene Associated with Familial 46,XX DSDYassine Naasse, Amina Bakhchane, Hicham Charoute, et al.
Pageof 10

Showing results (41-50 of 94) with videos related to

Sort By:
Pageof 10
Fertility and Sterility|May 26, 2009
Mutations in the TSPYL1 gene associated with 46,XY disorder of sex development and male infertilityGiovanna Vinci, Raja Brauner, Attila Tar, et al.
Human Molecular Genetics|February 20, 2014
Mutations in the FOG2/ZFPM2 gene are associated with anomalies of human testis determinationAnu Bashamboo, Raja Brauner, Joelle Bignon-Topalovic, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|July 31, 2014
A child with a novel de novo mutation in the aristaless domain of the aristaless-related homeobox (ARX) gene presenting with ambiguous genitalia and psychomotor delayNirmala Dushyanthi Sirisena, Kenneth McElreavey, Anu Bashamboo, et al.
Human Mutation|October 19, 2012
Unilateral cryptorchidism in mice mutant for PtgdsPascal Philibert, Brigitte Boizet-Bonhoure, Anu Bashamboo, et al.
Fertility and Sterility|October 5, 2010
Polymorphisms in MTHFR and MTRR genes associated with blood plasma homocysteine concentration and sperm countsDebbie Montjean, Moncef Benkhalifa, Lionel Dessolle, et al.
Gene|December 21, 2025
A novel candidate missense variant in the catalytic domain of USP26 associated with asthenoteratozoospermiaSeyedeh Zahra Mousavi, Masomeh Askari, Ken McElreavey, et al.
Fertility and Sterility|March 28, 2015
Genetic mutations and somatic anomalies in association with 46,XY gonadal dysgenesisClaire Bastian, Jean-Baptiste Muller, Stephen Lortat-Jacob, 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.
Plos One|July 2, 2010
Clinical, biological and genetic analysis of prepubertal isolated ovarian cyst in 11 girlsRaja Brauner, Anu Bashamboo, Sébastien Rouget, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|December 21, 2017
A Novel Homozygous Missense Mutation in the FU-CRD2 Domain of the R-spondin1 Gene Associated with Familial 46,XX DSDYassine Naasse, Amina Bakhchane, Hicham Charoute, et al.
Pageof 10