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English
Genetic heterogeneity associated with branchio-oto-renal syndrome
scientific article published on 01 March 1999
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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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