Cargando…

Proceedings of the 23(rd) Annual Meeting of the Portuguese Society of Human Genetics

Detalles Bibliográficos
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Wolters Kluwer Health 2020
Materias:	3500
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7478477/ http://dx.doi.org/10.1097/MD.0000000000019291

Ejemplares similares

Proceedings of the 24th Annual Meeting of the Portuguese Society of Human Genetics (SPGH – Sociedade Portuguesa de Genética Humana)
Publicado: (2021)

23rd Annual Meeting
Publicado: (2000)

Prenatal diagnosis of 7q11.23 microdeletion: Two cases report and literature review
por: Lv, Xin, et al.
Publicado: (2023)

Proceedings of the 25(th) Annual Meeting of the Portuguese Society of Human Genetics (SPGH – Sociedade Portuguesa de Genética Humana)
Publicado: (2022)

Clinicopathological and prognostic significance of NM23 expression in patients with non-small cell lung cancer: A systematic review and meta-analysis
por: Min, Shi-hui, et al.
Publicado: (2021)

Determinants of Plasma Renin Activity: Role of a Human Renin Gene Variant as a Genetic Factor
por: Konoshita, Tadashi, et al.
Publicado: (2014)

Association of IL-23R Polymorphisms (rs6682925, rs10889677, rs1884444) With Cancer Risk: A PRISMA-Compliant Meta-Analysis
por: Liu, Xing-Han, et al.
Publicado: (2015)

Common genetic variants in the FETUB locus, genetically predicted fetuin-B levels, and risk of insulin resistance in obese Chinese adults
por: Li, Zhibin, et al.
Publicado: (2017)

Clinical and Genetic Factors Associated With Thiazide-Induced Hyponatremia
por: Huang, Chin-Chou, et al.
Publicado: (2015)

Coexistence of t(2;14;11)(p16.1;q32;q23) and t(14;19)(q32;q13.3) chromosome translocations in a patient with chronic lymphocytic leukemia: A case report
por: Liu, Guangming, et al.
Publicado: (2017)

Thyroid hormone resistance and the value of genetics: Three case reports
por: Xiao, Xiao, et al.
Publicado: (2019)

Genetic variations associated with telomere length affect the risk of gastric carcinoma
por: Lili, Ma, et al.
Publicado: (2020)

Clinical and genetic features of four patients with Pearson syndrome: An observational study
por: Son, Ji Soo, et al.
Publicado: (2022)

Heme Oxygenase 1 and 2 Common Genetic Variants and Risk for Essential Tremor
por: Ayuso, Pedro, et al.
Publicado: (2015)

Association of Genetic Polymorphisms on VEGFA and VEGFR2 With Risk of Coronary Heart Disease
por: Liu, Doxing, et al.
Publicado: (2016)

Fibrodysplasia ossificans progressiva in a young adult with genetic mutation: Case report
por: Wang, Zhankui, et al.
Publicado: (2021)

Genetic Variations in Key MicroRNAs are Associated With the Survival of Nonsmall Cell Lung Cancer
por: Wu, Shuangshuang, et al.
Publicado: (2015)

Genetic analysis and management of a familial hypercholesterolemia pedigree with polygenic variants: Case report
por: Han, Yu, et al.
Publicado: (2023)

Multiple adverse drug reactions and genetic polymorphism testing: A case report with negative result
por: Arellano, Ana Lucía, et al.
Publicado: (2017)

Pharmacogenetic and case–control study on potassium channel related gene variants and genetic generalized epilepsy
por: Qu, Jian, et al.
Publicado: (2017)

Role of surfactant protein C in neonatal genetic disorders of the surfactant system: A case report
por: Tan, Ya-Xin, et al.
Publicado: (2021)

Clinical feature and genetic mutation of KBG syndrome diagnosed in neonatal period: A case report
por: Zhang, HaoZheng, et al.
Publicado: (2023)

Genetic testing involving 100 common mutations for antenatal diagnosis of hereditary hearing loss in Chongqing, China
por: Hu, Hua, et al.
Publicado: (2021)

Prenatal diagnosis and genetic analysis of a fetus with Branchio-oto-renal syndrome: A case report
por: Tang, Ping, et al.
Publicado: (2022)

Retrospective analysis of genetic etiology and obstetric outcome of fetal cystic hygroma: A single-center study
por: Cai, Meiying, et al.
Publicado: (2022)

Preimplantation genetic testing and prenatal diagnosis in a family with pseudovaginal perineoscrotal hypospadias: A case report
por: Chen, Jiayao, et al.
Publicado: (2023)

Phenotypic spectrum and genetic analysis in the fatal cases of Schaaf-Yang syndrome: Two case reports and literature review
por: Chen, Xuefei, et al.
Publicado: (2020)

Clinical and genetic factors associated with warfarin maintenance dose in northern Chinese patients with mechanical heart valve replacement
por: Liu, Rui, et al.
Publicado: (2017)

The combined effects of genetic risk and perceived discrimination on blood pressure among African Americans in the Jackson Heart Study
por: Taylor, Jacquelyn Y., et al.
Publicado: (2017)

Genetic polymorphisms of CYP3A4 among Chinese patients with steroid-induced osteonecrosis of the femoral head
por: Wang, Yuan, et al.
Publicado: (2016)

A multilocus genetic risk score for obesity: Association with BMI and metabolic alterations in a cohort with severe obesity
por: Sag, Sabine Julia Maria, et al.
Publicado: (2023)

Diagnostic performance of artificial intelligence to detect genetic diseases with facial phenotypes: A protocol for systematic review and meta analysis
por: Qin, Bosheng, et al.
Publicado: (2020)

Association between genetic polymorphisms of MMP8 and the risk of steroid-induced osteonecrosis of the femoral head in the population of northern China
por: Du, Jieli, et al.
Publicado: (2016)

A genetic variant in GLP1R is associated with response to DPP-4 inhibitors in patients with type 2 diabetes
por: Han, Eugene, et al.
Publicado: (2016)

Clinical and genetic analysis of 2 rare cases of Wiskott–Aldrich syndrome from Chinese minorities: Two case reports
por: Liu, Haifeng, et al.
Publicado: (2021)

The 23(rd) Annual Meeting of the European Tissue Repair Society (ETRS) in Reims, France
por: Von den Hoff, Johannes W, et al.
Publicado: (2014)

The genetic association between LMP2 and LMP7 polymorphisms and susceptibility of insulin dependent diabetes mellitus: A meta-analysis
por: Xu, Yang, et al.
Publicado: (2020)

Association Between Genetic Polymorphisms in the Promoter Regions of Let-7 and Risk of Papillary Thyroid Carcinoma: A Case-Control Study
por: Wang, Yichao, et al.
Publicado: (2015)

The genetic variants in calcium signaling related genes influence anti-tuberculosis drug induced liver injury: A prospective study
por: Lyu, Mengyuan, et al.
Publicado: (2019)

Genetically confirmed limb-girdle muscular dystrophy type 2B with DYSF mutation using gene panel sequencing: A case report
por: Lee, Sook Joung, et al.
Publicado: (2020)

Cannot write session to /tmp/vufind_sessions/sess_3pvnr1343i86i34k1cfio0kdu3