(Q67841749)

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

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

1 reference

X-linked nonsyndromic deafness

1 reference

1 reference

1 reference

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

22 November 2022

author name string

W. Reardon

1

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

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

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

22 November 2022

S. Bellman

5

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. Luxon

6

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

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

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

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

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

issue

4

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

page(s)

885-894

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

cites work

1

1 reference

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

X-linked progressive mixed deafness with perilymphatic gusher during stapes surgery.

22 November 2022

2

1 reference

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

Physical fine mapping of the choroideremia locus using Xq21 deletions associated with complex syndromes.

22 November 2022

4

1 reference

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

Cloning of a gene that is rearranged in patients with choroideraemia

22 November 2022

5

1 reference

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

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

22 November 2022

8

1 reference

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

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

22 November 2022

9

1 reference

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

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

22 November 2022

10

1 reference

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

22 November 2022

The stapes gusher.

11

1 reference

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

A rapid method for the purification of DNA from blood

22 November 2022

12

1 reference

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

Report of the committee on linkage and gene order

22 November 2022

13

1 reference

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

Usher syndrome: clinical findings and gene localization studies.

22 November 2022

14

1 reference

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

Localization of Usher syndrome type II to chromosome 1q.

22 November 2022

15

1 reference

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

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

22 November 2022

17

1 reference

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

Report of the committee on the genetic constitution of the X chromosome

22 November 2022

19

1 reference

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

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

22 November 2022

21

1 reference

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

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

22 November 2022

25

1 reference

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

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

22 November 2022

26

1 reference

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

Congenital deafness due to a sex-linked recessive gene

22 November 2022

27

1 reference

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

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

22 November 2022

29

1 reference

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

22 November 2022

The genetics of deafness

30

1 reference

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

22 November 2022

Sex-linked deaf-mutism

31

1 reference

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

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

22 November 2022

33

1 reference

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

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

22 November 2022

35

1 reference

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

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

22 November 2022

36

1 reference

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

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