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Andrew Dauber

Showing results (121-130 of 144) with videos related to

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The Journal of Clinical Investigation|October 17, 2023
OSR1 disruption contributes to uterine factor infertility via impaired Müllerian duct development and endometrial receptivityAdriana Lofrano-Porto, Sidney Alcântara Pereira, Andrew Dauber, et al.
European Journal of Endocrinology|October 17, 2025
EndoCompass project: research roadmap for growth disordersEvelien F Gevers, Anita C Hokken-Koelega, Maithe Tauber, et al.
Hormone Research in Paediatrics|December 1, 2025
EndoCompass Project: Research Roadmap for Growth DisordersEvelien F Gevers, Anita C Hokken-Koelega, Maithe Tauber, et al.
The Journal of Clinical Endocrinology and Metabolism|March 22, 2017
Paternally Inherited DLK1 Deletion Associated With Familial Central Precocious PubertyAndrew Dauber, Marina Cunha-Silva, Delanie B Macedo, et al.
EMBO Molecular Medicine|February 24, 2016
Mutations in pregnancy-associated plasma protein A2 cause short stature due to low IGF-I availabilityAndrew Dauber, María T Muñoz-Calvo, Vicente Barrios, et al.
Nature Genetics|November 28, 2018
Gain-of-function DNMT3A mutations cause microcephalic dwarfism and hypermethylation of Polycomb-regulated regionsPatricia Heyn, Clare V Logan, Adeline Fluteau, et al.
The New England Journal of Medicine|June 7, 2013
Central precocious puberty caused by mutations in the imprinted gene MKRN3Ana Paula Abreu, Andrew Dauber, Delanie B Macedo, et al.
The Journal of Pediatrics|October 22, 2019
Genetic Disorders in Prenatal Onset Syndromic Short Stature Identified by Exome SequencingThais Kataoka Homma, Bruna Lucheze Freire, Rachel Sayuri Honjo Kawahira, et al.
Endocrine Reviews|January 13, 2023
International Consensus Guideline on Small for Gestational Age: Etiology and Management From Infancy to Early AdulthoodAnita C S Hokken-Koelega, Manouk van der Steen, Margaret C S Boguszewski, et al.
The Journal of Clinical Endocrinology and Metabolism|March 18, 2014
Central precocious puberty that appears to be sporadic caused by paternally inherited mutations in the imprinted gene makorin ring finger 3Delanie B Macedo, Ana Paula Abreu, Ana Claudia S Reis, et al.
Pageof 15

Showing results (121-130 of 144) with videos related to

Sort By:
Pageof 15
The Journal of Clinical Investigation|October 17, 2023
OSR1 disruption contributes to uterine factor infertility via impaired Müllerian duct development and endometrial receptivityAdriana Lofrano-Porto, Sidney Alcântara Pereira, Andrew Dauber, et al.
European Journal of Endocrinology|October 17, 2025
EndoCompass project: research roadmap for growth disordersEvelien F Gevers, Anita C Hokken-Koelega, Maithe Tauber, et al.
Hormone Research in Paediatrics|December 1, 2025
EndoCompass Project: Research Roadmap for Growth DisordersEvelien F Gevers, Anita C Hokken-Koelega, Maithe Tauber, et al.
The Journal of Clinical Endocrinology and Metabolism|March 22, 2017
Paternally Inherited DLK1 Deletion Associated With Familial Central Precocious PubertyAndrew Dauber, Marina Cunha-Silva, Delanie B Macedo, et al.
EMBO Molecular Medicine|February 24, 2016
Mutations in pregnancy-associated plasma protein A2 cause short stature due to low IGF-I availabilityAndrew Dauber, María T Muñoz-Calvo, Vicente Barrios, et al.
Nature Genetics|November 28, 2018
Gain-of-function DNMT3A mutations cause microcephalic dwarfism and hypermethylation of Polycomb-regulated regionsPatricia Heyn, Clare V Logan, Adeline Fluteau, et al.
The New England Journal of Medicine|June 7, 2013
Central precocious puberty caused by mutations in the imprinted gene MKRN3Ana Paula Abreu, Andrew Dauber, Delanie B Macedo, et al.
The Journal of Pediatrics|October 22, 2019
Genetic Disorders in Prenatal Onset Syndromic Short Stature Identified by Exome SequencingThais Kataoka Homma, Bruna Lucheze Freire, Rachel Sayuri Honjo Kawahira, et al.
Endocrine Reviews|January 13, 2023
International Consensus Guideline on Small for Gestational Age: Etiology and Management From Infancy to Early AdulthoodAnita C S Hokken-Koelega, Manouk van der Steen, Margaret C S Boguszewski, et al.
The Journal of Clinical Endocrinology and Metabolism|March 18, 2014
Central precocious puberty that appears to be sporadic caused by paternally inherited mutations in the imprinted gene makorin ring finger 3Delanie B Macedo, Ana Paula Abreu, Ana Claudia S Reis, et al.
Pageof 15