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A rapid systematic review of outcomes studies in genetic counseling
As healthcare reimbursement is increasingly tied to value‐of‐service, it is critical for the
genetic counselor (GC) profession to demonstrate the value added by GCs through …
genetic counselor (GC) profession to demonstrate the value added by GCs through …
Genetic testing for congenital non-syndromic sensorineural hearing loss
Introduction Approximately 60% of congenital pediatric hearing loss is of genetic etiology. To
evaluate non-syndromic sensorineural hearing loss (NSSNHL), guidelines emphasize the …
evaluate non-syndromic sensorineural hearing loss (NSSNHL), guidelines emphasize the …
Mutations in GJB2 as major causes of autosomal recessive non-syndromic hearing loss: first report of c. 299-300delAT mutation in Kurdish population of Iran
Background and Objectives Autosomal recessive non-syndromic hearing loss (ARNSHL)
with genetic origin is common (1/2000 births). ARNSHL can be associated with mutations in …
with genetic origin is common (1/2000 births). ARNSHL can be associated with mutations in …
Using video technology to engage deaf sign language users in survey research: An example from the'Insign'project
For many deaf signers, a signed language is their first or preferred language; spoken or
written languages are often second languages and literacy levels among deaf signers vary …
written languages are often second languages and literacy levels among deaf signers vary …
Genetic testing hearing loss: The challenge of non syndromic mimics
Congenital hearing loss is a common cause of morbidity in early childhood. There are
multiple reasons for congenital hearing impairment, with genetic contribution becoming …
multiple reasons for congenital hearing impairment, with genetic contribution becoming …
Towards cultural competence in the genomic age: A review of current health care provider educational trainings and interventions
Abstract Purpose of Review The increasing diversity of the USA brings opportunities and
challenges for health care providers, health care systems, and policymakers to create and …
challenges for health care providers, health care systems, and policymakers to create and …
Personal utility of genomic sequencing for infants with congenital deafness
Decisions about genetic testing have traditionally been based on clinical utility and cost, but
personal utility is increasingly recognized when assessing the value of testing. Whole …
personal utility is increasingly recognized when assessing the value of testing. Whole …
The role of educational experiences in enhancing the cultural identity of deaf and hard-of-hearing undergraduate female students in Saudi Arabia
This study explored how educational experiences enhance the cultural identity of deaf and
hard-of-hearing undergraduate female students in Saudi Arabia, using an explanatory …
hard-of-hearing undergraduate female students in Saudi Arabia, using an explanatory …
[HTML][HTML] Ethical issues associated with preconception genetic screening: historical experience and current trends
AE Donnikov - Obstetrics and gynecology, 2019 - en.aig-journal.ru
The discovery of molecular markers for hereditary diseases and the development of
technologies that made genetic diagnosis accessible to a wide range of people have …
technologies that made genetic diagnosis accessible to a wide range of people have …
Этические вопросы, связанные с преконцепционным генетическим скринингом: исторический опыт и современные тенденции
АЕ Донников - Акушерство и гинекология, 2019 - elibrary.ru
Открытие молекулярных маркеров наследственных болезней и развитие технологий,
сделавших генетическую диагностику доступной широким слоям населения, создали …
сделавших генетическую диагностику доступной широким слоям населения, создали …