Prenatal diagnosis for inherited deafness--what is the potential demand? (Q48653289)

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scientific article published in April 2001

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Language	Label	Description	Also known as
English	Prenatal diagnosis for inherited deafness--what is the potential demand?	scientific article published in April 2001

Statements

instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11767801

reference URL

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

retrieved

5 December 2019

title

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

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11767801

reference URL

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

retrieved

5 December 2019

main subject

deafness

1 reference

based on heuristic

inferred from title

author

Anna Middleton

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11767801

reference URL

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

retrieved

5 December 2019

author name string

J Hewison

series ordinal

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11767801

reference URL

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

retrieved

5 December 2019

R Mueller

series ordinal

3

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11767801

reference URL

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

retrieved

5 December 2019

publication date

1 April 2001

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11767801

reference URL

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

retrieved

5 December 2019

published in

Journal of Genetic Counseling

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11767801

reference URL

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

retrieved

5 December 2019

volume

10

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11767801

reference URL

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

retrieved

5 December 2019

issue

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11767801

reference URL

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

retrieved

5 December 2019

page(s)

121-131

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11767801

reference URL

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

retrieved

5 December 2019

cites work

Genetic counseling of the deaf. Medical and cultural considerations

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11767801

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11767801

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Connexin 26 gene mutation and autosomal recessive deafness

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11767801

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Attitudes of deaf adults toward genetic testing for hereditary deafness

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11767801

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11767801

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic causes of nonsyndromic hearing loss

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11767801

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ethical issues in prenatal testing

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11767801

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ethical issues in the genetic study of deafness

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11767801

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Effectiveness of genetic testing in certain diseases must be evaluated

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11767801

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11767801

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetics and molecular biology of deafness

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11767801

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ethical and legal implications of advances in genetic testing technology.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11767801

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11767801

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1023/A:1009439630457

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11767801

reference URL

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

retrieved

5 December 2019

PubMed publication ID

11767801

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11767801

reference URL

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

retrieved

5 December 2019

 

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