不满分子
发表于 2025-3-28 17:27:39
,Inherited Ocular Disease in the New Zealand Māori: Novel Genetic Mechanisms and Founder Effects,ovel variants in many genes. Understanding the population-specific genetic disease spectrum and clinical phenotypes, as well as a knowledge of regional ancestry and iwi (tribe), aids in simplifying the diagnostic process.
珐琅
发表于 2025-3-28 21:32:48
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TOXIC
发表于 2025-3-29 00:45:08
Unique Patient Populations in Asia for Genetic Eye Research,tant for better diagnosis and management of eye diseases. Each population is accompanied by a unique patient data set and needs elaborate and well divided study. Area wise description of patient population in Asia for genetic eye research has been provided in the following chapter.
nonchalance
发表于 2025-3-29 05:38:48
Retina Genes in Chinese,pulations. We have investigated ., ., ., ., ., ., ., ., and other genes in Chinese patients with retinal diseases including age-related macular degeneration, polypoidal choroidal vasculopathy diabetic retinopathy, retinitis pigmentosa, Best vitelliform macular dystrophy, and Stargardt disease.
懒惰人民
发表于 2025-3-29 08:23:27
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镇压
发表于 2025-3-29 12:14:59
,eyeGENE®: A Model for Advancing Research of Rare, Inherited Eye Conditions Through Biobanking and D improved our understanding of inherited eye disease, and validated new molecular diagnostic technology. eyeGENE. can serve as a model for creating a research resource to advance the study of rare, inherited diseases.
虚假
发表于 2025-3-29 17:07:57
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食品室
发表于 2025-3-29 20:11:57
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挫败
发表于 2025-3-30 02:23:06
Book 2019n of information on genetic eye research in western countries, more than sixty percent of the human genes involved in eye diseases in the Asian and Pacific population remain unknown. However, new efforts and a new awareness have sparked important discussions on the subject, and new plans are being i
脱离
发表于 2025-3-30 05:31:13
Richard Savage,Michael Stauntonpulations, the NGO sector can be an ally in building the capacity for research among service providers. This chapter frames this opportunity and offers recommendations to genetics researchers who seek to broaden their array of research options.