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English
Maternal isodisomy of chromosome 9 with no impact on the phenotype in a woman with two isochromosomes: i(9p) and i(9q)
scientific article published on 01 November 1999
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scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10528247
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10528247%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 November 2019
title
Maternal isodisomy of chromosome 9 with no impact on the phenotype in a woman with two isochromosomes: i(9p) and i(9q)
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10528247
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10528247%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 November 2019
main subject
Isodisomy
1 reference
based on heuristic
inferred from title
phenotype
1 reference
based on heuristic
inferred from title
author name string
E J Björck
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10528247
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10528247%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 November 2019
B M Anderlid
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10528247
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10528247%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 November 2019
E Blennow
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10528247
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10528247%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 November 2019
publication date
1 November 1999
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10528247
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10528247%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 November 2019
published in
American Journal of Medical Genetics Part A
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10528247
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10528247%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 November 2019
volume
87
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10528247
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10528247%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 November 2019
issue
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10528247
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10528247%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 November 2019
page(s)
49-52
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10528247
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10528247%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 November 2019
cites work
Fifty probands with extra structurally abnormal chromosomes characterized by fluorescence in situ hybridization
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819991105%2987%3A1%3C49%3A%3AAID-AJMG10%3E3.0.CO%3B2-4
retrieved
21 January 2018
Paternal uniparental disomy for chromosome 14: a case report and review
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819991105%2987%3A1%3C49%3A%3AAID-AJMG10%3E3.0.CO%3B2-4
retrieved
21 January 2018
Molecular studies in 37 Silver-Russell syndrome patients: frequency and etiology of uniparental disomy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819991105%2987%3A1%3C49%3A%3AAID-AJMG10%3E3.0.CO%3B2-4
retrieved
21 January 2018
Maternal uniparental disomy of chromosome 1 with no apparent phenotypic effects
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819991105%2987%3A1%3C49%3A%3AAID-AJMG10%3E3.0.CO%3B2-4
retrieved
21 January 2018
Uniparental disomy 7 in Silver-Russell syndrome and primordial growth retardation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819991105%2987%3A1%3C49%3A%3AAID-AJMG10%3E3.0.CO%3B2-4
retrieved
21 January 2018
Uniparental disomy in humans: development of an imprinting map and its implications for prenatal diagnosis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819991105%2987%3A1%3C49%3A%3AAID-AJMG10%3E3.0.CO%3B2-4
retrieved
21 January 2018
A comprehensive human linkage map with centimorgan density. Cooperative Human Linkage Center (CHLC)
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819991105%2987%3A1%3C49%3A%3AAID-AJMG10%3E3.0.CO%3B2-4
retrieved
21 January 2018
Whole-arm translocation between homologous chromosomes 7 in a woman with successive spontaneous abortions
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819991105%2987%3A1%3C49%3A%3AAID-AJMG10%3E3.0.CO%3B2-4
retrieved
21 January 2018
A human chromosome 9-specific alphoid DNA repeat spatially resolvable from satellite 3 DNA by fluorescent in situ hybridization.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819991105%2987%3A1%3C49%3A%3AAID-AJMG10%3E3.0.CO%3B2-4
retrieved
21 January 2018
Is there an abnormal phenotype associated with maternal isodisomy for chromosome 2 in the presence of two isochromosomes?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819991105%2987%3A1%3C49%3A%3AAID-AJMG10%3E3.0.CO%3B2-4
retrieved
21 January 2018
Mosaic uniparental disomy in Beckwith-Wiedemann syndrome.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819991105%2987%3A1%3C49%3A%3AAID-AJMG10%3E3.0.CO%3B2-4
retrieved
21 January 2018
A case of maternal uniparental disomy of chromosome 9 in association with confined placental mosaicism for trisomy 9
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819991105%2987%3A1%3C49%3A%3AAID-AJMG10%3E3.0.CO%3B2-4
retrieved
21 January 2018
A male with trisomy 9 mosaicism and maternal uniparental disomy for chromosome 9 in the euploid cell line
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819991105%2987%3A1%3C49%3A%3AAID-AJMG10%3E3.0.CO%3B2-4
retrieved
21 January 2018
Identifiers
DOI
10.1002/(SICI)1096-8628(19991105)87:1<49::AID-AJMG10>3.0.CO;2-4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10528247
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10528247%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 November 2019
PubMed publication ID
10528247
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10528247
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10528247%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 November 2019
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