A multipedigree linkage study of X-linked deafness: Linkage to Xq13-q21 and evidence for genetic heterogeneity (Q67841749)

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18 September 2019

title

A multipedigree linkage study of X-linked deafness: linkage to Xq13-q21 and evidence for genetic heterogeneity (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1783396%20AND%20SRC:MED&resulttype=core&format=json

18 September 2019

A multipedigree linkage study of X-linked deafness: Linkage to Xq13-q21 and evidence for genetic heterogeneity (English)

1 reference

https://api.crossref.org/works/10.1016/0888-7543(91)90011-3

22 November 2022

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X-linked nonsyndromic deafness

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1 reference

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https://api.crossref.org/works/10.1016/0888-7543(91)90011-3

22 November 2022

author name string

W. Reardon

1

1 reference

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22 November 2022

H. R. Middleton-Price

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1783396

22 November 2022

L. Sandkuijl

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1783396

22 November 2022

P. Phelps

4

1 reference

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22 November 2022

S. Bellman

5

1 reference

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22 November 2022

L. Luxon

6

1 reference

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22 November 2022

M. E. Pembrey

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1783396

22 November 2022

S. Malcolm

8

1 reference

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22 November 2022

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=1783396

22 November 2022

publication date

1 December 1991

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1783396%20AND%20SRC:MED&resulttype=core&format=json

full work available at URL

18 September 2019

https://api.elsevier.com/content/article/PII:0888754391900113?httpAccept=text/xml

1 reference

https://api.crossref.org/works/10.1016/0888-7543(91)90011-3

https://api.elsevier.com/content/article/PII:0888754391900113?httpAccept=text/plain

22 November 2022

1 reference

https://api.crossref.org/works/10.1016/0888-7543(91)90011-3

22 November 2022

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1783396%20AND%20SRC:MED&resulttype=core&format=json

18 September 2019

volume

11

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18 September 2019

page(s)

885-894

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18 September 2019

issue

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1783396%20AND%20SRC:MED&resulttype=core&format=json

The gene for X-linked progressive mixed deafness with perilymphatic gusher during stapes surgery (DFN3) is linked to PGK

18 September 2019

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22 November 2022

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A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity

22 November 2022

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22 November 2022

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Sex-linked recessive congenital deafness and the excess of males in profound childhood deafness

22 November 2022

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22 November 2022

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A rapid method for the purification of DNA from blood

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22 November 2022

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22 November 2022

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Localization of Usher syndrome type II to chromosome 1q.

22 November 2022

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Mapping recessive ophthalmic diseases: linkage of the locus for Usher syndrome type II to a DNA marker on chromosome 1q.

22 November 2022

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22 November 2022

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Choroideremia and deafness with stapes fixation: a contiguous gene deletion syndrome in Xq21

22 November 2022

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X-linked mixed deafness with congenital fixation of the stapedial footplate and perilymphatic gusher

22 November 2022

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Localizing multiple X chromosome-linked retinitis pigmentosa loci using multilocus homogeneity tests

22 November 2022

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Congenital deafness due to a sex-linked recessive gene

22 November 2022

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X-linked deafness, stapes gushers and a distinctive defect of the inner ear.

22 November 2022

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22 November 2022

The genetics of deafness

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22 November 2022

Sex-linked deaf-mutism

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Regional localization of polymorphic DNA loci on the proximal long arm of the X chromosome using deletions associated with choroideremia

22 November 2022

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X-linked mixed deafness with stapes fixation in a Mauritian kindred: linkage to Xq probe pDP34.

22 November 2022

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X-linked inheritance of ocular albinism with late-onset sensorineural deafness.

22 November 2022

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22 November 2022

Identifiers

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1783396%20AND%20SRC:MED&resulttype=core&format=json

18 September 2019

1 reference