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Anu Bashamboo

Showing results (21-30 of 94) with videos related to

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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|June 16, 2017
A novel HSD17B3 gene mutation in a 46,XY female-phenotype newborn identified by whole-exome sequencingRita Bertalan, Osnat Admoni, Anu Bashamboo, et al.
DNA and Cell Biology|September 24, 2004
Organizational variation of DYZ1 repeat sequences on the human Y chromosome and its diagnostic potentialsMohammed Mahidur Rahman, Anu Bashamboo, Aparna Prasad, et al.
The Journal of Clinical Endocrinology and Metabolism|April 13, 2017
Mutations in the Human ROBO1 Gene in Pituitary Stalk Interruption SyndromeAnu Bashamboo, Joelle Bignon-Topalovic, Nasser Moussi, et al.
European Journal of Pediatrics|November 27, 2014
Etiology of primary ovarian insufficiency in a series young girls presenting at a pediatric endocrinology centerRaja Brauner, Sophie Pierrepont, Joelle Bignon-Topalovic, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 12, 2011
Loss-of-function mutation in GATA4 causes anomalies of human testicular developmentDiana Lourenço, Raja Brauner, Magda Rybczynska, et al.
Frontiers in Endocrinology|April 18, 2022
Disorders of Sex Development in a Large Ukrainian Cohort: Clinical Diversity and Genetic FindingsEvgenia Globa, Natalia Zelinska, Yulia Shcherbak, et al.
Plos One|August 20, 2011
Clinical, biological and genetic analysis of anorchia in 26 boysRaja Brauner, Mathieu Neve, Slimane Allali, et al.
Molecular Human Reproduction|December 8, 2004
Fate of SRY, PABY, DYS1, DYZ3 and DYZ1 loci in Indian patients harbouring sex chromosomal anomaliesAnu Bashamboo, Mohammed Mahidur Rahman, Aparna Prasad, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|November 17, 2025
Bilateral Testicular Regression Syndrome and Optic Nerve Atrophy: Clinical Aspects of a Child with a <italic>SEMA3E</italic> Loss-of-Function VariantSomboon Wankanit, Maëva Elzaiat, Estelle Talouarn, et al.
Pageof 10

Showing results (21-30 of 94) with videos related to

Sort By:
Pageof 10
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|June 16, 2017
A novel HSD17B3 gene mutation in a 46,XY female-phenotype newborn identified by whole-exome sequencingRita Bertalan, Osnat Admoni, Anu Bashamboo, et al.
DNA and Cell Biology|September 24, 2004
Organizational variation of DYZ1 repeat sequences on the human Y chromosome and its diagnostic potentialsMohammed Mahidur Rahman, Anu Bashamboo, Aparna Prasad, et al.
The Journal of Clinical Endocrinology and Metabolism|April 13, 2017
Mutations in the Human ROBO1 Gene in Pituitary Stalk Interruption SyndromeAnu Bashamboo, Joelle Bignon-Topalovic, Nasser Moussi, et al.
European Journal of Pediatrics|November 27, 2014
Etiology of primary ovarian insufficiency in a series young girls presenting at a pediatric endocrinology centerRaja Brauner, Sophie Pierrepont, Joelle Bignon-Topalovic, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 12, 2011
Loss-of-function mutation in GATA4 causes anomalies of human testicular developmentDiana Lourenço, Raja Brauner, Magda Rybczynska, et al.
Frontiers in Endocrinology|April 18, 2022
Disorders of Sex Development in a Large Ukrainian Cohort: Clinical Diversity and Genetic FindingsEvgenia Globa, Natalia Zelinska, Yulia Shcherbak, et al.
Plos One|August 20, 2011
Clinical, biological and genetic analysis of anorchia in 26 boysRaja Brauner, Mathieu Neve, Slimane Allali, et al.
Molecular Human Reproduction|December 8, 2004
Fate of SRY, PABY, DYS1, DYZ3 and DYZ1 loci in Indian patients harbouring sex chromosomal anomaliesAnu Bashamboo, Mohammed Mahidur Rahman, Aparna Prasad, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|November 17, 2025
Bilateral Testicular Regression Syndrome and Optic Nerve Atrophy: Clinical Aspects of a Child with a <italic>SEMA3E</italic> Loss-of-Function VariantSomboon Wankanit, Maëva Elzaiat, Estelle Talouarn, et al.
Pageof 10