Genetic heterogeneity associated with branchio-oto-renal syndrome (Q74650984)

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scientific article published on 01 March 1999

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Language	Label	Description	Also known as
English	Genetic heterogeneity associated with branchio-oto-renal syndrome	scientific article published on 01 March 1999

Statements

instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PubMed publication ID

10096598

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10096598%20AND%20SRC:MED&resulttype=core&format=json

retrieved

12 November 2019

title

Genetic heterogeneity associated with branchio-oto-renal syndrome (English)

1 reference

stated in

Europe PubMed Central

PubMed publication ID

10096598

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10096598%20AND%20SRC:MED&resulttype=core&format=json

retrieved

12 November 2019

main subject

heterogeneity

1 reference

based on heuristic

inferred from title

author name string

S Kumar

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

10096598

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10096598%20AND%20SRC:MED&resulttype=core&format=json

retrieved

12 November 2019

W J Kimberling

series ordinal

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

10096598

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10096598%20AND%20SRC:MED&resulttype=core&format=json

retrieved

12 November 2019

H A Marres

series ordinal

3

1 reference

stated in

Europe PubMed Central

PubMed publication ID

10096598

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10096598%20AND%20SRC:MED&resulttype=core&format=json

retrieved

12 November 2019

C W Cremers

series ordinal

4

1 reference

stated in

Europe PubMed Central

PubMed publication ID

10096598

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10096598%20AND%20SRC:MED&resulttype=core&format=json

retrieved

12 November 2019

publication date

1 March 1999

1 reference

stated in

Europe PubMed Central

PubMed publication ID

10096598

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10096598%20AND%20SRC:MED&resulttype=core&format=json

retrieved

12 November 2019

published in

American Journal of Medical Genetics Part A

1 reference

stated in

Europe PubMed Central

PubMed publication ID

10096598

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10096598%20AND%20SRC:MED&resulttype=core&format=json

retrieved

12 November 2019

volume

83

1 reference

stated in

Europe PubMed Central

PubMed publication ID

10096598

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10096598%20AND%20SRC:MED&resulttype=core&format=json

retrieved

12 November 2019

issue

3

1 reference

stated in

Europe PubMed Central

PubMed publication ID

10096598

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10096598%20AND%20SRC:MED&resulttype=core&format=json

retrieved

12 November 2019

page(s)

207-208

1 reference

stated in

Europe PubMed Central

PubMed publication ID

10096598

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10096598%20AND%20SRC:MED&resulttype=core&format=json

retrieved

12 November 2019

cites work

The earpits-deafness syndrome. Clinical and genetic aspects

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990319%2983%3A3%3C207%3A%3AAID-AJMG12%3E3.0.CO%3B2-A

retrieved

21 January 2018

Otological aspects of the earpit-deafness syndrome

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990319%2983%3A3%3C207%3A%3AAID-AJMG12%3E3.0.CO%3B2-A

retrieved

21 January 2018

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

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990319%2983%3A3%3C207%3A%3AAID-AJMG12%3E3.0.CO%3B2-A

retrieved

21 January 2018

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

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990319%2983%3A3%3C207%3A%3AAID-AJMG12%3E3.0.CO%3B2-A

retrieved

21 January 2018

New autosomal dominant branchio-oculo-facial syndrome

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990319%2983%3A3%3C207%3A%3AAID-AJMG12%3E3.0.CO%3B2-A

retrieved

21 January 2018

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

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990319%2983%3A3%3C207%3A%3AAID-AJMG12%3E3.0.CO%3B2-A

retrieved

21 January 2018

Branchio-oto-renal syndrome: identification of novel mutations, molecular characterization, mutation distribution, and prospects for genetic testing

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990319%2983%3A3%3C207%3A%3AAID-AJMG12%3E3.0.CO%3B2-A

retrieved

21 January 2018

The branchio-oculo-facial syndrome

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990319%2983%3A3%3C207%3A%3AAID-AJMG12%3E3.0.CO%3B2-A

retrieved

21 January 2018

Congenital Conductive or Mixed Deafness, Preauricular Sinus, External Ear Anomaly, and Commissural Lip Pits: An Autosomal Dominant Inherited Syndrome

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990319%2983%3A3%3C207%3A%3AAID-AJMG12%3E3.0.CO%3B2-A

retrieved

21 January 2018

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

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990319%2983%3A3%3C207%3A%3AAID-AJMG12%3E3.0.CO%3B2-A

retrieved

21 January 2018

Identifiers

DOI

10.1002/(SICI)1096-8628(19990319)83:3<207::AID-AJMG12>3.0.CO;2-A

1 reference

stated in

Europe PubMed Central

PubMed publication ID

10096598

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10096598%20AND%20SRC:MED&resulttype=core&format=json

retrieved

12 November 2019

PubMed publication ID

10096598

1 reference

stated in

Europe PubMed Central

PubMed publication ID

10096598

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10096598%20AND%20SRC:MED&resulttype=core&format=json

retrieved

12 November 2019

 

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