Results 11 to 20 of about 17,949 (246)

Análisis de la causalidad en el estudio genético de los trastornos neuropsiquiátricos: revisión narrativa

open access: yesMedicina U.P.B., 2017
Los trastornos neuropsiquiátricos se caracterizan por formas complejas de transmisión genética. El conocimiento de los aspectos básicos de los diseños metodológicos más usados en la investigación sobre la genética de estos trastornos permite al clínico ...
Ana Milena Gaviria Gómez
doaj   +1 more source

Orthodontics and Genetics

open access: yesDental Press Journal of Orthodontics, 2019
Introduction: Genetics has been suggested as an explanation for the etiology of malocclusions, although some questions, due to the perception that genetic inheritance is tied to a monogenic or Mendelian form of inheritance.
Alexandre R. Vieira
doaj   +1 more source

Multiple abnormalities in a foetus: a possibility of multifactorial inheritance disorder

open access: yesNational Journal of Clinical Anatomy, 2016
A female foetus of 3.23 kg was delivered by a primigravida of 23 years, after scanning by ultrasound, depicting findings of oligohydramnios and congenital abnormalities.
D N Sinha
doaj   +1 more source

Risk factors for major external structural birth defects among children in Kiambu County, Kenya: a case-control study [version 2; peer review: 1 approved, 2 approved with reservations]

open access: yesF1000Research, 2021
Background: Although major external structural birth defects continue to occur globally, the greatest burden is shouldered by resource-constrained countries with no surveillance systems.
George N. Agot   +2 more
doaj   +1 more source

The role of family history as a risk factor for non-syndromic cleft lip and/or palate with multifactorial inheritance

open access: yesDental Journal, 2021
Background: Cleft lip with or without cleft palate (CL/P) is a facial growth ‘disorder that occurs during gestation and has multifactorial causes owing to both genetic and environmental factors.
Agung Sosiawan   +4 more
doaj   +1 more source

Familial Segregation of Venous Thromboembolism in Sweden: A Nationwide Family Study of Heritability and Complex Segregation Analysis

open access: yesJournal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, 2021
Background This is the first nationwide segregation analysis that aimed to determine whether familial venous thromboembolism (VTE) is attributable to inheritance and/or shared environment, and the possible mode of inheritance.
Bengt Zöller   +8 more
doaj   +1 more source

Inheritance patterns of localized aggressive periodontitis: A systematic review

open access: yesJournal of Indian Association of Public Health Dentistry, 2017
Inheritance patterns are traits/diseases that are passed from parents to offspring through genes. Elucidation of inheritance pattern of localized aggressive periodontitis may permit us to have a better understanding of the disease etiology, thereby ...
Jaseela Praveena   +4 more
doaj   +1 more source

Genital Vulvar Lichen Sclerosus in Monozygotic Twin Women: A Case Report and Review of the Literature

open access: yesCase Reports in Dermatology, 2013
Lichen sclerosus et atrophicus is a skin disease of multifactorial etiology which appears in patients with genetic or hormonal predisposition and autoimmune disease.
Georgeta Doulaveri   +4 more
doaj   +1 more source

Advance Genome Disorder Prediction Model Empowered With Deep Learning

open access: yesIEEE Access, 2022
A major and essential issue in biomedical research is to predict genome disorder. Genome disorders cause multivariate diseases like cancer, dementia, diabetes, cystic fibrosis, leigh syndrome, etc.
Atta-Ur-Rahman   +7 more
doaj   +1 more source

A substitution mutation in LRP8 gene is significantly associated with susceptibility to familial myocardial infarction [PDF]

open access: yesARYA Atherosclerosis, 2020
BACKGROUND: Myocardial infarction (MI) is a multifactorial disease caused by the suspension of blood circulation in a part of the myocardium. Understanding the genetic basis of MI can provide insight regarding the pathogenesis of the disease.
Mohammad Javad Ghorbani   +4 more
doaj   +1 more source

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