(Q48616316)

13 February 2018

title

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

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13 February 2018

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Orit Dagan

1

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13 February 2018

Hagit Hochner

2

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13 February 2018

Haya Levi

3

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13 February 2018

Annick Raas-Rothschild

4

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13 February 2018

Michal Sagi

5

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13 February 2018

publication date

1 November 2002

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13 February 2018

American Journal of Medical Genetics Part A

published in

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13 February 2018

volume

113

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13 February 2018

issue

2

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13 February 2018

page(s)

137-143

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13 February 2018

Screening for carriers of Tay-Sachs disease in the ultraorthodox Ashkenazi Jewish community in Israel.

cites work

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10676

Parental attitudes toward genetic testing for pediatric deafness

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10676

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10676

Contribution of connexin 26 mutations to nonsyndromic deafness in Ashkenazi patients and the variable phenotypic effect of the mutation 167delT.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10676

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10676

Attitudes of deaf adults toward genetic testing for hereditary deafness

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10676

Genetic epidemiology of hearing impairment

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10676

Perceptions of Ashkenazi Jewish breast cancer patients on genetic testing for mutations in BRCA1 and BRCA2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10676

Ethical aspects of genetic screening in Israel

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10676

The prevalence and expression of inherited connexin 26 mutations associated with nonsyndromic hearing loss in the Israeli population

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10676

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10676

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10676

Innovative approach to genetic counseling services for the deaf population

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10676

Application of the Health Belief Model in a study on parents' intentions to utilize prenatal diagnosis of cleft lip and/or palate

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10676

Amniocentesis rate and the detection of Down syndrome and other chromosomal anomalies in Israel

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10676

21 January 2018

Identifiers

DOI

10.1002/AJMG.10676

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13 February 2018

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13 February 2018