(Q46321973)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17952575%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

title

Ethnic differences in parental perceptions of genetic testing for deaf infants (English)

1 reference

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9 January 2020

6

1 reference

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9 January 2020

author name string

Christina G S Palmer

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17952575%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

Ariadna Martinez

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17952575%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

Michelle Fox

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17952575%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

Yvonne Sininger

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17952575%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

Wayne W Grody

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17952575%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

publication date

19 October 2007

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17952575%20AND%20SRC:MED&resulttype=core&format=json

Journal of Genetic Counseling

9 January 2020

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17952575%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

volume

17

1 reference

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9 January 2020

issue

1

1 reference

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9 January 2020

page(s)

129-138

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17952575%20AND%20SRC:MED&resulttype=core&format=json

Connexin 26 Gene Mutations in Congenitally Deaf Children

9 January 2020

cites work

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS10897-007-9134-Z

Genetic testing as part of the early hearing detection and intervention (EHDI) process.

21 January 2018

1 reference

12 December 2020

Controlled trial of pretest education approaches to enhance informed decision-making for BRCA1 gene testing.

1 reference

12 December 2020

GJB2 (connexin 26) variants and nonsyndromic sensorineural hearing loss: a HuGE review

1 reference

12 December 2020

Genetic testing for hearing loss: different motivations for the same outcome.

1 reference

12 December 2020

A focus group study of consumer attitudes toward genetic testing and newborn screening for deafness.

1 reference

12 December 2020

Genetic epidemiology of hearing impairment

1 reference

12 December 2020

Novel mutations in the connexin 26 gene (GJB2) that cause autosomal recessive (DFNB1) hearing loss

1 reference

12 December 2020

A deletion involving the connexin 30 gene in nonsyndromic hearing impairment

1 reference

12 December 2020

Language of early- and later-identified children with hearing loss.

1 reference

12 December 2020

A deletion mutation in GJB6 cooperating with a GJB2 mutation in trans in non-syndromic deafness: A novel founder mutation in Ashkenazi Jews

1 reference

12 December 2020

Molecular genetics of hearing impairment due to mutations in gap junction genes encoding beta connexins

1 reference

12 December 2020

Racial and ethnic variations in knowledge and attitudes about genetic testing

1 reference

12 December 2020

Attitudes of deaf adults toward genetic testing for hereditary deafness

1 reference

12 December 2020

Connexin 26 mutations in hereditary non-syndromic sensorineural deafness

1 reference

12 December 2020

Connexin26 mutations associated with the most common form of non-syndromic neurosensory autosomal recessive deafness (DFNB1) in Mediterraneans

1 reference

12 December 2020

Racial differences in beliefs about genetic screening among patients at inner-city neighborhood health centers.

1 reference

12 December 2020

Comparing knowledge and attitudes towards genetic testing in Parkinson's disease in an American and Asian population.

1 reference

12 December 2020

Genetics Evaluation Guidelines for the Etiologic Diagnosis of Congenital Hearing Loss. Genetic Evaluation of Congenital Hearing Loss Expert Panel. ACMG statement

1 reference

12 December 2020

Exploring the complexities of familism and acculturation: central constructs for people of Mexican origin

1 reference

12 December 2020

Parental narratives on genetic testing for children with hearing loss: a qualitative inquiry

1 reference

12 December 2020

Attitudes of deaf individuals towards genetic testing

1 reference

12 December 2020

Carrier rates in the midwestern United States for GJB2 mutations causing inherited deafness.

1 reference

12 December 2020

Molecular basis of childhood deafness resulting from mutations in the GJB2 (connexin 26) gene.

1 reference

12 December 2020

Ethical principles and cultural integrity in health care delivery: Asian ethnocultural perspectives in genetic services

1 reference

12 December 2020

Genetic testing for hereditary hearing loss: connexin 26 (GJB2) allele variants and two novel deafness-causing mutations (R32C and 645-648delTAGA).

1 reference

12 December 2020

Attitudes of the broader hearing, deaf, and hard-of-hearing community toward genetic testing for deafness.

1 reference

12 December 2020

Attitudes toward genetic testing among the general population and relatives of patients with a severe genetic disease: a survey from Finland.

1 reference

12 December 2020

A novel service delivery model for infant hearing screening in developing countries

1 reference

12 December 2020

Parental attitudes toward genetic testing for pediatric deafness

1 reference

12 December 2020

Correlates of intentions to obtain genetic counseling and colorectal cancer gene testing among at-risk relatives from three ethnic groups.

1 reference

12 December 2020

Perceived disadvantages and concerns about abuses of genetic testing for cancer risk: differences across African American, Latina and Caucasian women

1 reference

12 December 2020

Prelingual deafness: high prevalence of a 30delG mutation in the connexin 26 gene

1 reference

12 December 2020

Universal neonatal hearing screening moving from evidence to practice

1 reference

12 December 2020

Prevalence and evolutionary origins of the del(GJB6-D13S1830) mutation in the DFNB1 locus in hearing-impaired subjects: a multicenter study

1 reference

12 December 2020

Newborn hearing screening--a silent revolution

1 reference

12 December 2020

Differences between African Americans and Whites in their attitudes toward genetic testing for Alzheimer's disease

1 reference

12 December 2020

10.1007/S10897-007-9134-Z

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17952575%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

1 reference