(Q69927658)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2904400%20AND%20SRC:MED&resulttype=core&format=json

7 October 2019

title

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

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2904400%20AND%20SRC:MED&resulttype=core&format=json

7 October 2019

1 reference

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2904400%20AND%20SRC:MED&resulttype=core&format=json

7 October 2019

author name string

H G Brunner

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2904400%20AND%20SRC:MED&resulttype=core&format=json

7 October 2019

A van Bennekom

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2904400%20AND%20SRC:MED&resulttype=core&format=json

7 October 2019

T L Oei

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2904400%20AND%20SRC:MED&resulttype=core&format=json

7 October 2019

W R Cremers

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2904400%20AND%20SRC:MED&resulttype=core&format=json

7 October 2019

B Wieringa

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2904400%20AND%20SRC:MED&resulttype=core&format=json

7 October 2019

H H Ropers

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2904400%20AND%20SRC:MED&resulttype=core&format=json

7 October 2019

publication date

1 December 1988

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2904400%20AND%20SRC:MED&resulttype=core&format=json

7 October 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2904400%20AND%20SRC:MED&resulttype=core&format=json

7 October 2019

volume

80

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2904400%20AND%20SRC:MED&resulttype=core&format=json

7 October 2019

issue

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2904400%20AND%20SRC:MED&resulttype=core&format=json

7 October 2019

page(s)

337-340

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2904400%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1007/bf00273647

7 October 2019

exact match

0 references

cites work

Choroideremia, obesity, and congenital deafness

1 reference

12 December 2020

A strategy to reveal high-frequency RFLPs along the human X chromosome

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12 December 2020

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

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X-linked deafness in a South African kindred

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12 December 2020

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

1 reference

12 December 2020

Audiologic features of the X-linked progressive mixed deafness syndrome with perilymphatic gusher during stapes gusher.

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Clinical features of female heterozygotes in the X-linked mixed deafness syndrome (with perilymphatic gusher during stapes surgery).

1 reference

12 December 2020

Deletion of the DXS165 locus in patients with classical choroideremia

1 reference

12 December 2020

Easy calculations of lod scores and genetic risks on small computers

1 reference

12 December 2020

PROFOUND CHILDHOOD DEAFNESS.

1 reference

12 December 2020

Genetic mapping of nine DNA markers in the q11----q22 region of the human X chromosome

1 reference

12 December 2020

Isolation of anonymous DNA sequences from within a submicroscopic X chromosomal deletion in a patient with choroideremia, deafness, and mental retardation

1 reference

12 December 2020

Choroideremia, congenital deafness and mental retardation in a family with an X chromosomal deletion.

1 reference

12 December 2020