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Clinical Endocrinology|September 7, 2007
Seminiferous tubule function in delayed-onset X-linked adrenal hypoplasia congenita associated with incomplete hypogonadotrophic hypogonadismIgnacio Bergadá, Luz Andreone, Patricia Bedecarrás, et al.Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|November 2, 2013
Sequence analysis of the ADRA2A coding region in children affected by attention deficit hyperactivity disorderTaryn Castro, Heidi Eliana Mateus, Dora Janeth Fonseca, et al.Pediatric Endocrinology Reviews : PER|October 7, 2005
Premature ovarian failure and forkhead transcription factor FOXL2: blepharophimosis-ptosis-epicanthus inversus syndrome and ovarian dysfunctionElfride De Baere, Silvia Copelli, Sandrine Caburet, et al.Plos One|August 24, 2012
Refined mapping of a quantitative trait locus on chromosome 1 responsible for mouse embryonic deathMagalie Vatin, Gaetan Burgio, Gilles Renault, et al.Reproductive Biomedicine Online|January 31, 2012
Screening for mutations of the FOXO4 gene in premature ovarian failure patientsDora Janeth Fonseca, Eliana Garzón, Besma Lakhal, et al.Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|August 13, 2003
Undertreatment strongly decreases prognosis of breast cancer in elderly womenChristine Bouchardy, Elisabetta Rapiti, Gérald Fioretta, et al.Pharmacogenomics and Personalized Medicine|March 19, 2020
A Pharmacogenomic Dissection of a Rosuvastatin-Induced Rhabdomyolysis Case Evokes the Polygenic Nature of Adverse Drug ReactionsCarlos Alberto Calderon-Ospina, Mario Hernández-Sómerson, Ana María García, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 19, 2018
ATG7 and ATG9A loss-of-function variants trigger autophagy impairment and ovarian failureClémence Delcour, Larbi Amazit, Liliana C Patino, et al.BMC Research Notes|October 28, 2017
A first description of the Colombian national registry for rare diseasesHeidi Eliana Mateus, Ana María Pérez, Martha Lucía Mesa, et al.Plos One|October 11, 2017
Novel genes and mutations in patients affected by recurrent pregnancy lossPaula Quintero-Ronderos, Eric Mercier, Michiko Fukuda, et al.Pageof 7