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English
Prenatal diagnosis of mosaic ring chromosome 13 with anencephaly
scientific article published on 01 February 2001
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scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11241535
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11241535%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 November 2019
title
Prenatal diagnosis of mosaic ring chromosome 13 with anencephaly
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11241535
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11241535%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 November 2019
author name string
C P Chen
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11241535
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11241535%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 November 2019
S R Chern
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11241535
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11241535%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 November 2019
C C Lee
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11241535
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11241535%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 November 2019
W L Chen
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11241535
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11241535%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 November 2019
W Wang
series ordinal
5
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11241535
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11241535%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 November 2019
publication date
1 February 2001
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11241535
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11241535%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 November 2019
published in
Prenatal Diagnosis
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11241535
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11241535%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 November 2019
volume
21
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11241535
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11241535%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 November 2019
issue
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11241535
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11241535%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 November 2019
page(s)
102-105
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11241535
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11241535%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 November 2019
cites work
Prenatally detected fetal myelomeningocele: is karyotype analysis warranted?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F1097-0223%28200102%2921%3A2%3C102%3A%3AAID-PD992%3E3.0.CO%3B2-5
retrieved
21 January 2018
A fetus with a chromosome 13 ring and placenta with chromosome 13 rod/ring mosaicism
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F1097-0223%28200102%2921%3A2%3C102%3A%3AAID-PD992%3E3.0.CO%3B2-5
retrieved
21 January 2018
Ring chromosome 13: lack of distinct syndromes based on different breakpoints on 13q
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F1097-0223%28200102%2921%3A2%3C102%3A%3AAID-PD992%3E3.0.CO%3B2-5
retrieved
21 January 2018
Preliminary definition of a "critical region" of chromosome 13 in q32: report of 14 cases with 13q deletions and review of the literature.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F1097-0223%28200102%2921%3A2%3C102%3A%3AAID-PD992%3E3.0.CO%3B2-5
retrieved
21 January 2018
Holoprosencephaly due to mutations in ZIC2, a homologue of Drosophila odd-paired
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F1097-0223%28200102%2921%3A2%3C102%3A%3AAID-PD992%3E3.0.CO%3B2-5
retrieved
21 January 2018
Apparent lability of neural tube closure in laboratory animals and humans
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reference URL
https://api.crossref.org/works/10.1002%2F1097-0223%28200102%2921%3A2%3C102%3A%3AAID-PD992%3E3.0.CO%3B2-5
retrieved
21 January 2018
Familial partial trisomy of the long arm of chromosome 3 (3q)
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F1097-0223%28200102%2921%3A2%3C102%3A%3AAID-PD992%3E3.0.CO%3B2-5
retrieved
21 January 2018
Neural tube and craniofacial defects with special emphasis on folate pathway genes.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1002%2F1097-0223%28200102%2921%3A2%3C102%3A%3AAID-PD992%3E3.0.CO%3B2-5
retrieved
21 January 2018
Mosaic r(13) in an infant with aprosencephaly
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F1097-0223%28200102%2921%3A2%3C102%3A%3AAID-PD992%3E3.0.CO%3B2-5
retrieved
21 January 2018
Aneuploidy among prenatally detected neural tube defects
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F1097-0223%28200102%2921%3A2%3C102%3A%3AAID-PD992%3E3.0.CO%3B2-5
retrieved
21 January 2018
Prenatally diagnosed neural tube defects: ultrasound, chromosome, and autopsy or postnatal findings in 212 cases
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1002%2F1097-0223%28200102%2921%3A2%3C102%3A%3AAID-PD992%3E3.0.CO%3B2-5
retrieved
21 January 2018
Neural tube defects and the 13q deletion syndrome: evidence for a critical region in 13q33-34.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F1097-0223%28200102%2921%3A2%3C102%3A%3AAID-PD992%3E3.0.CO%3B2-5
retrieved
21 January 2018
5,10 Methylenetetrahydrofolate reductase genetic polymorphism as a risk factor for neural tube defects
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F1097-0223%28200102%2921%3A2%3C102%3A%3AAID-PD992%3E3.0.CO%3B2-5
retrieved
21 January 2018
Fetal karyotype following ascertainment of fetal anomalies by ultrasound
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F1097-0223%28200102%2921%3A2%3C102%3A%3AAID-PD992%3E3.0.CO%3B2-5
retrieved
21 January 2018
Mutated methylenetetrahydrofolate reductase as a risk factor for spina bifida
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F1097-0223%28200102%2921%3A2%3C102%3A%3AAID-PD992%3E3.0.CO%3B2-5
retrieved
21 January 2018
Identifiers
DOI
10.1002/1097-0223(200102)21:2<102::AID-PD992>3.0.CO;2-5
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11241535
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11241535%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 November 2019
PubMed publication ID
11241535
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11241535
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11241535%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 November 2019
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