(Q77428741)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9777487%20AND%20SRC:MED&resulttype=core&format=json

5 December 2019

review article

1 reference

title

Branchio-oto-renal syndrome (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9777487%20AND%20SRC:MED&resulttype=core&format=json

5 December 2019

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9777487%20AND%20SRC:MED&resulttype=core&format=json

5 December 2019

author name string

C Schwartz

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9777487%20AND%20SRC:MED&resulttype=core&format=json

5 December 2019

publication date

1 September 1998

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9777487%20AND%20SRC:MED&resulttype=core&format=json

Journal of Communication Disorders

5 December 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9777487%20AND%20SRC:MED&resulttype=core&format=json

5 December 2019

volume

31

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9777487%20AND%20SRC:MED&resulttype=core&format=json

5 December 2019

issue

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9777487%20AND%20SRC:MED&resulttype=core&format=json

5 December 2019

page(s)

411-20; quiz 421

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9777487%20AND%20SRC:MED&resulttype=core&format=json

A human homologue of the Drosophila eyes absent gene underlies branchio-oto-renal (BOR) syndrome and identifies a novel gene family

5 December 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9924%2898%2900013-6

The eyes absent gene: genetic control of cell survival and differentiation in the developing Drosophila eye.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9924%2898%2900013-6

Embryology of the sheep. II. The alimentary tract and associated glands

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9924%2898%2900013-6

The branchio-oto-renal (BOR) syndrome: report of bilateral renal agenesis in three sibs

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9924%2898%2900013-6

Phenotypic manifestations of branchio-oto-renal syndrome.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9924%2898%2900013-6

Branchio-oto-renal syndrome: further delineation of an underdiagnosed syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9924%2898%2900013-6

The earpits-deafness syndrome. Clinical and genetic aspects.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9924%2898%2900013-6

Neo-oval window technique and myringo-chorda-vestibulopexy in the BOR syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9924%2898%2900013-6

Otological aspects of the earpit-deafness syndrome.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9924%2898%2900013-6

The Temporal Bone in the Preauricular Pit, Cervical Fistula, Hearing Loss Syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9924%2898%2900013-6

Autosomal dominant duplication of the renal collecting system, hearing loss, and external ear anomalies: a new syndrome?

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9924%2898%2900013-6

Genetic aspects of the BOR syndrome—branchial fistulas, ear pits, hearing loss, and renal anomalies

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9924%2898%2900013-6

Frequency of the branchio-oto-renal (BOR) syndrome in children with profound hearing loss.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9924%2898%2900013-6

Branchio-oto-renal dysplasia in three families.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9924%2898%2900013-6

The BOR syndrome and renal agenesis--prenatal diagnosis and further clinical delineation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9924%2898%2900013-6

Tricho-rhino-phalangeal and branchio-oto syndromes in a family with an inherited rearrangement of chromosome 8q.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9924%2898%2900013-6

Branchio-oto-renal syndrome: reduced penetrance and variable expressivity in four generations of a large kindred

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9924%2898%2900013-6

Apoptosis in metanephric development

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9924%2898%2900013-6

Autosomal dominant branchio-oto-renal syndrome--localization of a disease gene to chromosome 8q by linkage in a Dutch family

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9924%2898%2900013-6

Branchio-oto-renal dysplasia and branchio-oto dysplasia: two distinct autosomal dominant disorders.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9924%2898%2900013-6

Computed tomography of earpits-deafness syndrome.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9924%2898%2900013-6

Refined localization of the branchiootorenal syndrome gene by linkage and haplotype analysis.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9924%2898%2900013-6

Localization of the gene for branchiootorenal syndrome to chromosome 8q.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9924%2898%2900013-6

A proposed new contiguous gene syndrome on 8q consists of Branchio-Oto-Renal (BOR) syndrome, Duane syndrome, a dominant form of hydrocephalus and trapeze aplasia; implications for the mapping of the BOR gene.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9924%2898%2900013-6

Localization of branchio-oto-renal (BOR) syndrome to a 3 Mb region of chromosome 8q

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9924%2898%2900013-6

10.1016/S0021-9924(98)00013-6

7 January 2021

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9777487%20AND%20SRC:MED&resulttype=core&format=json

5 December 2019

1 reference