Results 11 to 20 of about 22,844 (195)
Dentistry Case Simulator: Amelogenesis Imperfecta (Out of Print)
Introduction Researchers at the University of Michigan School Of Dentistry, along with genetics leaders from across the country, collaborated in designing the Genetics Education in Dentistry Case Simulator to integrate genetics into existing dental ...
Jan Hu +6 more
doaj +1 more source
In the 1920s and 30s, significant empirical studies were undertaken on mixed-race (‘hybrid’) populations in Britain’s seaport communities.
Peter J. Aspinall
doaj +1 more source
Genealogy study of three generations of patients with bipolar mood disorder Type I
Introduction: The purpose of this research is genealogy examination of three generation of bipolar mood disorder Type I patients. Methods: Patients selected using Poisson sampling method from 100 patients with bipolar mood disorder Type I, referring to a
Bahman Salehi +4 more
doaj +1 more source
Background The Tohoku Medical Megabank project aims to create a next-generation personalized healthcare system by conducting large-scale genome-cohort studies involving three generations of local residents in the areas affected by the Great East Japan ...
Tomoharu Tokutomi +5 more
doaj +1 more source
The persistent horns are an important trait of speciation for the family Bovidae with complex morphogenesis taking place briefly after birth. The polledness is highly favourable in modern cattle breeding systems but serious animal welfare issues urge for
Blum, Helmut +8 more
core +1 more source
Genetic Analysis of Oculocutaneous Albinism Type1A (OCA1A) in an Iranian Family [PDF]
Background: Oculocutaneous albinism type1 (OCA1) is characterized by the absence of melanin pigmentation. The mutation on TYR gene makes OCA1 as an autosomal recessive genetic disorder.
H Pour-Jafari +2 more
doaj +1 more source
Further genetic heterogeneity for autosomal dominant human sutural cataracts [PDF]
A unique sutural cataract was observed in a 4-generation German family to be transmitted as an isolated autosomal, dominant trait. Since mutations in the gamma-crystallin encoding CRYG genes have previously been demonstrated to be the most frequent ...
Billingsley, G. +6 more
core +1 more source
Best vitelliform macular dystrophy in a large Brazilian family
Background To describe the clinical and multimodal imaging findings of a Brazilian family with Best vitelliform macular dystrophy. Methods A retrospective chart review of a Brazilian family was conducted and complementary fundus images (color photography,
Carolina Pádua Rocha de Souza +3 more
doaj +1 more source
Background The CDC's Family History Public Health Initiative encourages adoption and increase awareness of family health history. To meet these goals and develop a personalized medicine implementation science research agenda, the Genomedical Connection ...
Agbaje Astrid B +8 more
doaj +1 more source
PBL Case on Child Abuse/Hemophilia A
This resource includes a problem-based learning (PBL) case on the dichotomy of child abuse and hemophilia A. The author's preferred implementation of the case had instructors handing out the first four pages of the case in Session #1, the following six ...
Niels Larsen +5 more
doaj +1 more source

