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English
Second 46,XX male with MLS syndrome
scientific article published on 01 February 1998
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9508062
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9508062%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 November 2019
title
Second 46,XX male with MLS syndrome
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9508062
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9508062%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 November 2019
author name string
R F Stratton
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9508062
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9508062%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 November 2019
C A Walter
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9508062
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9508062%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 November 2019
B R Paulgar
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9508062
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9508062%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 November 2019
M E Price
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9508062
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9508062%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 November 2019
C M Moore
series ordinal
5
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9508062
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9508062%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 November 2019
publication date
1 February 1998
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9508062
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9508062%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 November 2019
published in
American Journal of Medical Genetics Part A
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9508062
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9508062%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 November 2019
volume
76
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9508062
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9508062%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 November 2019
issue
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9508062
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9508062%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 November 2019
page(s)
37-41
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9508062
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9508062%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 November 2019
cites work
Linear skin defects and congenital microphthalmia: a new syndrome at Xp22.2.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980226%2976%3A1%3C37%3A%3AAID-AJMG6%3E3.0.CO%3B2-M
retrieved
21 January 2018
MLS, Aicardi and Goltz syndromes: how many genes involved?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980226%2976%3A1%3C37%3A%3AAID-AJMG6%3E3.0.CO%3B2-M
retrieved
21 January 2018
Female infant with oncocytic cardiomyopathy and microphthalmia with linear skin defects (MLS): a clue to the pathogenesis of oncocytic cardiomyopathy?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980226%2976%3A1%3C37%3A%3AAID-AJMG6%3E3.0.CO%3B2-M
retrieved
21 January 2018
Clinical, cytogenetic, and pedigree findings in 18 cases of Aicardi syndrome.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980226%2976%3A1%3C37%3A%3AAID-AJMG6%3E3.0.CO%3B2-M
retrieved
21 January 2018
Microphthalmia and chorioretinal lesions in a girl with an Xp22.2-pter deletion and partial 3p trisomy: clinical observations relevant to Aicardi syndrome gene localization
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980226%2976%3A1%3C37%3A%3AAID-AJMG6%3E3.0.CO%3B2-M
retrieved
21 January 2018
MIDAS syndrome (microphthalmia, dermal aplasia, and sclerocornea): an X-linked phenotype distinct from Goltz syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980226%2976%3A1%3C37%3A%3AAID-AJMG6%3E3.0.CO%3B2-M
retrieved
21 January 2018
Histopathological study of focal dermal hypoplasia (Goltz syndrome).
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980226%2976%3A1%3C37%3A%3AAID-AJMG6%3E3.0.CO%3B2-M
retrieved
21 January 2018
Pathologic features of myocardial hamartomas causing childhood tachyarrhythmias
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980226%2976%3A1%3C37%3A%3AAID-AJMG6%3E3.0.CO%3B2-M
retrieved
21 January 2018
Xp22.3 microdeletion syndrome with microphthalmia, sclerocornea, linear skin defects, and congenital heart defects
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980226%2976%3A1%3C37%3A%3AAID-AJMG6%3E3.0.CO%3B2-M
retrieved
21 January 2018
Microphthalmia with linear skin defects (MLS) syndrome: clinical, cytogenetic, and molecular characterization.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980226%2976%3A1%3C37%3A%3AAID-AJMG6%3E3.0.CO%3B2-M
retrieved
21 January 2018
MIDAS syndrome respectively MLS syndrome: a separate entity rather than a particular lyonization pattern of the gene causing Goltz syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980226%2976%3A1%3C37%3A%3AAID-AJMG6%3E3.0.CO%3B2-M
retrieved
21 January 2018
Combined Goltz and Aicardi syndromes in a terminal Xp deletion: are they a contiguous gene syndrome?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980226%2976%3A1%3C37%3A%3AAID-AJMG6%3E3.0.CO%3B2-M
retrieved
21 January 2018
Aicardi syndrome: early neuroradiological manifestations and results of DNA studies in one patient
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980226%2976%3A1%3C37%3A%3AAID-AJMG6%3E3.0.CO%3B2-M
retrieved
21 January 2018
Early detection of canine ceroid-lipofuscinosis (CCL): an ultrastructural study
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980226%2976%3A1%3C37%3A%3AAID-AJMG6%3E3.0.CO%3B2-M
retrieved
21 January 2018
Oncocytic cardiomyopathy in an infant with oncocytosis in exocrine and endocrine glands.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980226%2976%3A1%3C37%3A%3AAID-AJMG6%3E3.0.CO%3B2-M
retrieved
21 January 2018
De novo deletion of Xp22.2-pter in a female with linear skin lesions of the face and neck, microphthalmia, and anterior chamber eye anomalies
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980226%2976%3A1%3C37%3A%3AAID-AJMG6%3E3.0.CO%3B2-M
retrieved
21 January 2018
A YAC-based binning strategy facilitating the rapid assembly of cosmid contigs: 1.6 Mb of overlapping cosmids in Xp22.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980226%2976%3A1%3C37%3A%3AAID-AJMG6%3E3.0.CO%3B2-M
retrieved
21 January 2018
Identifiers
DOI
10.1002/(SICI)1096-8628(19980226)76:1<37::AID-AJMG6>3.0.CO;2-M
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9508062
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9508062%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 November 2019
PubMed publication ID
9508062
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9508062
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9508062%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 November 2019
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