(Q70961925)

English

Infantile variant of Bartter syndrome and sensorineural deafness: a new autosomal recessive disorder

scientific article published on 01 December 1995

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Europe PubMed Central

PubMed publication ID

8585565

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8585565%20AND%20SRC:MED&resulttype=core&format=json

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15 October 2019

title

Infantile variant of Bartter syndrome and sensorineural deafness: a new autosomal recessive disorder (English)

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Europe PubMed Central

PubMed publication ID

8585565

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8585565%20AND%20SRC:MED&resulttype=core&format=json

15 October 2019

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Landau D

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Europe PubMed Central

PubMed publication ID

8585565

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8585565%20AND%20SRC:MED&resulttype=core&format=json

retrieved

15 October 2019

Shalev H

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2

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Europe PubMed Central

PubMed publication ID

8585565

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8585565%20AND%20SRC:MED&resulttype=core&format=json

retrieved

15 October 2019

Ohaly M

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3

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8585565

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15 October 2019

Carmi R

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4

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PubMed publication ID

8585565

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15 October 2019

publication date

1 December 1995

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Europe PubMed Central

PubMed publication ID

8585565

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8585565%20AND%20SRC:MED&resulttype=core&format=json

retrieved

15 October 2019

published in

American Journal of Medical Genetics Part A

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Europe PubMed Central

PubMed publication ID

8585565

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8585565%20AND%20SRC:MED&resulttype=core&format=json

retrieved

15 October 2019

volume

59

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Europe PubMed Central

PubMed publication ID

8585565

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8585565%20AND%20SRC:MED&resulttype=core&format=json

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15 October 2019

issue

4

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Europe PubMed Central

PubMed publication ID

8585565

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8585565%20AND%20SRC:MED&resulttype=core&format=json

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15 October 2019

page(s)

454-459

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Europe PubMed Central

PubMed publication ID

8585565

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8585565%20AND%20SRC:MED&resulttype=core&format=json

retrieved

15 October 2019

Identifiers

DOI

10.1002/AJMG.1320590411

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stated in

Europe PubMed Central

PubMed publication ID

8585565

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8585565%20AND%20SRC:MED&resulttype=core&format=json

retrieved

15 October 2019

PubMed publication ID

8585565

1 reference

stated in

Europe PubMed Central

PubMed publication ID

8585565

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8585565%20AND%20SRC:MED&resulttype=core&format=json

(Q70961925)

Infantile variant of Bartter syndrome and sensorineural deafness: a new autosomal recessive disorder

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