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Reproductive Sciences (Thousand Oaks, Calif.)|March 19, 2019
Genetic Variants Contributing to Early Recurrent Pregnancy Loss Etiology Identified by Sequencing ApproachesPaula Quintero-Ronderos, Paul LaissueJournal of Molecular Medicine (Berlin, Germany)|July 1, 2018
The multisystemic functions of FOXD1 in development and diseasePaula Quintero-Ronderos, Paul LaissueReproductive Sciences (Thousand Oaks, Calif.)|May 21, 2020
Genetic Variants Contributing to Early Recurrent Pregnancy Loss Etiology Identified by Sequencing ApproachesPaula Quintero-Ronderos, Paul LaissueAutoimmune Diseases|April 27, 2012
Epigenetics and autoimmune diseasesPaula Quintero-Ronderos, Gladis Montoya-OrtizPlos One|October 11, 2017
Novel genes and mutations in patients affected by recurrent pregnancy lossPaula Quintero-Ronderos, Eric Mercier, Michiko Fukuda, et al.Reproductive Biology and Endocrinology : RB&E|December 3, 2017
THBD sequence variants potentially related to recurrent pregnancy lossPaula Quintero-Ronderos, Eric Mercier, Jean-Christophe Gris, et al.Molecular and Cellular Endocrinology|July 27, 2017
The molecular complexity of primary ovarian insufficiency aetiology and the use of massively parallel sequencingPaul LaissueMolecular and Cellular Endocrinology|May 12, 2015
Aetiological coding sequence variants in non-syndromic premature ovarian failure: From genetic linkage analysis to next generation sequencingPaul LaissueMolecular Cancer|January 10, 2019
The forkhead-box family of transcription factors: key molecular players in colorectal cancer pathogenesisPaul LaissueMolecular Medicine (Cambridge, Mass.)|August 10, 2019
FOXD1 mutations are related to repeated implantation failure, intra-uterine growth restriction and preeclampsiaPaula Quintero-Ronderos, Karen Marcela Jiménez, Clara Esteban-Pérez, et al.Pageof 7