(Q48653289)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11767801%20AND%20SRC:MED&resulttype=core&format=json

5 December 2019

title

Prenatal diagnosis for inherited deafness--what is the potential demand? (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11767801%20AND%20SRC:MED&resulttype=core&format=json

5 December 2019

1 reference

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11767801%20AND%20SRC:MED&resulttype=core&format=json

5 December 2019

author name string

J Hewison

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11767801%20AND%20SRC:MED&resulttype=core&format=json

5 December 2019

R Mueller

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11767801%20AND%20SRC:MED&resulttype=core&format=json

5 December 2019

publication date

1 April 2001

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11767801%20AND%20SRC:MED&resulttype=core&format=json

Journal of Genetic Counseling

5 December 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11767801%20AND%20SRC:MED&resulttype=core&format=json

5 December 2019

volume

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11767801%20AND%20SRC:MED&resulttype=core&format=json

5 December 2019

issue

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11767801%20AND%20SRC:MED&resulttype=core&format=json

5 December 2019

page(s)

121-131

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11767801%20AND%20SRC:MED&resulttype=core&format=json

Genetic counseling of the deaf. Medical and cultural considerations

5 December 2019

cites work

1 reference

12 December 2020

Genetic dilemmas and the child's right to an open future

1 reference

12 December 2020

Connexin 26 gene mutation and autosomal recessive deafness

1 reference

12 December 2020

Attitudes of deaf adults toward genetic testing for hereditary deafness

1 reference

12 December 2020

Clinical phenotype and mutations in connexin 26 (DFNB1/GJB2), the most common cause of childhood hearing loss

1 reference

12 December 2020

Genetic causes of nonsyndromic hearing loss

1 reference

12 December 2020

Ethical issues in prenatal testing

1 reference

12 December 2020

Ethical issues in the genetic study of deafness

1 reference

12 December 2020

Effectiveness of genetic testing in certain diseases must be evaluated

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

Genetics and molecular biology of deafness

1 reference

12 December 2020

Ethical and legal implications of advances in genetic testing technology.

1 reference

12 December 2020

Ethical issues related to prenatal genetic testing. The Council on Ethical and Judicial Affairs, American Medical Association

1 reference

12 December 2020

Identifiers

DOI

10.1023/A:1009439630457

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11767801%20AND%20SRC:MED&resulttype=core&format=json

5 December 2019

1 reference