Human Genome Epidemiology Literature Finder
Records 1 - 12 (of 12 Records) |
Query Trace: Syndrome and POR[original query] |
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[Genetic predisposition and Pediatric Acute Respiratory Distress Syndrome: New tools for genetic study]. Revista chilena de pediatri?a 0 86 (2): 73-9. Erranz M Benjamín, Wilhelm B Jan, Riquelme V Raquel, Cruces R Pab |
[Turner syndrome and genetic polymorphism: a systematic review]. Revista paulista de pediatria : orga?o oficial da Sociedade de Pediatria de Sa?o Paulo 2015 Sep 33 (3): 364-71. Trovó de Marqui Alessandra Bernade |
Population Pharmacokinetics of Prednisolone in Relation to Clinical Outcome in Children With Nephrotic Syndrome. Therapeutic drug monitoring 2016 Apr . Teeninga Nynke, Guan Zheng, Stevens Jasper, Kist-van Holthe Joana E, Ackermans Mariëtte T, van der Heijden Albert J, van Schaik Ron H N, van Gelder Teun, Nauta Jero |
Paraoxonase 1 (Q192R) gene polymorphism, coronary heart disease and the risk of a new acute coronary event. Clinica e investigacion en arteriosclerosis : publicacion oficial de la Sociedad Espanola de Arteriosclerosis 2016 Nov . Martínez-Quintana Efrén, Rodríguez-González Fayna, Medina-Gil José María, Garay-Sánchez Paloma, Tugores Anton |
FMR1 expression in human granulosa cells increases with exon 1 CGG repeat length depending on ovarian reserve. Reproductive biology and endocrinology : RB&E 2018 7 16 (1): 65. Rehnitz Julia, Alcoba Diego D, Brum Ilma S, Dietrich Jens E, Youness Berthe, Hinderhofer Katrin, Messmer Birgitta, Freis Alexander, Strowitzki Thomas, Germeyer Aria |
[Molecular autopsy in sudden cardiac death]. Archivos de cardiologia de Mexico 2018 7 88 (4): 306-312. Bonilla Juan Carlos, Parra-Medina Rafael, Chaves Juan José, Campuzano Oscar, Sarquella-Brugada Georgia, Brugada Ramón, Brugada Jos |
Association of a cholesteryl ester transfer protein variant (rs1800777) with fat mass, HDL cholesterol levels, and metabolic syndrome. Endocrinologia, diabetes y nutricion 2018 Apr . de Luis Daniel, Izaola Olatz, Primo David, Gomez Emilia, Lopez Juan Jose, Ortola Ana, Aller Roc |
[Endothelin-1 rs5370 gene polymorphism in primary nephrotic syndrome: A case-control study]. Anales de pediatria 2020 Dec . Rizk Hoda, Hammad Ayman, El-Said Afaf, Wahba Yah |
Secondary hypertriglyceridemia. Clinica e investigacion en arteriosclerosis : publicacion oficial de la Sociedad Espanola de Arteriosclerosis 2021 5 33 Suppl 2 29-36. Viñals Clara, Zambón Daniel, Yago Gema, Domenech Mònica, Ortega Emil |
[Clinical Characteristics and Genetic Analysis of Klippel-Feil Syndrome]. Zhongguo yi xue ke xue yuan xue bao. Acta Academiae Medicinae Sinicae 2021 3 43 (1): 25-31. Li Zi Quan, Geng Mo Zhao, Zhao Sen, Wu Zhi Hong, Zhang Jian Guo, Wu Nan, Wang Yi Pe |
A spectrum of recessiveness among Mendelian disease variants in UK Biobank. American journal of human genetics 2022 May . Barton Alison R, Hujoel Margaux L A, Mukamel Ronen E, Sherman Maxwell A, Loh Po- |
Poor Ovarian Response to Gonadotrophins in PCOS Women after Laparoscopic Ovarian Drilling. Medicina (Kaunas, Lithuania) 2022 2 58 (2): . Burnik Papler Tanja, Stimpfel Martin, Kovacik Brina, Bokal Eda Vrtacn |
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- Page last updated:Apr 22, 2024
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