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Fryns syndrome phenotype and trisomy 22
scientific article published on 01 January 1996
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8741922
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8741922%20AND%20SRC:MED&resulttype=core&format=json
retrieved
18 October 2019
title
Fryns syndrome phenotype and trisomy 22
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8741922
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8741922%20AND%20SRC:MED&resulttype=core&format=json
retrieved
18 October 2019
main subject
Fryns syndrome
1 reference
based on heuristic
inferred from title
phenotype
1 reference
based on heuristic
inferred from title
author name string
Ladonne JM
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8741922
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8741922%20AND%20SRC:MED&resulttype=core&format=json
retrieved
18 October 2019
Gaillard D
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8741922
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8741922%20AND%20SRC:MED&resulttype=core&format=json
retrieved
18 October 2019
Carré-Pigeon F
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8741922
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8741922%20AND%20SRC:MED&resulttype=core&format=json
retrieved
18 October 2019
Gabriel R
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8741922
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8741922%20AND%20SRC:MED&resulttype=core&format=json
retrieved
18 October 2019
publication date
1 January 1996
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8741922
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8741922%20AND%20SRC:MED&resulttype=core&format=json
retrieved
18 October 2019
published in
American Journal of Medical Genetics Part A
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8741922
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8741922%20AND%20SRC:MED&resulttype=core&format=json
retrieved
18 October 2019
volume
61
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8741922
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8741922%20AND%20SRC:MED&resulttype=core&format=json
retrieved
18 October 2019
issue
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8741922
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8741922%20AND%20SRC:MED&resulttype=core&format=json
retrieved
18 October 2019
page(s)
68-70
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8741922
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8741922%20AND%20SRC:MED&resulttype=core&format=json
retrieved
18 October 2019
cites work
Fryns syndrome: report on 8 new cases
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960102%2961%3A1%3C68%3A%3AAID-AJMG13%3E3.0.CO%3B2-U
retrieved
21 January 2018
Congenital diaphragmatic hernia, coarse facies, and acral hypoplasia: Fryns syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960102%2961%3A1%3C68%3A%3AAID-AJMG13%3E3.0.CO%3B2-U
retrieved
21 January 2018
Diaphragmatic hernia in tetrasomy 12p mosaicism
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960102%2961%3A1%3C68%3A%3AAID-AJMG13%3E3.0.CO%3B2-U
retrieved
21 January 2018
Cystic hygroma and congenital diaphragmatic hernia: early prenatal sonographic evaluation of Fryns' syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960102%2961%3A1%3C68%3A%3AAID-AJMG13%3E3.0.CO%3B2-U
retrieved
21 January 2018
A new lethal syndrome with cloudy corneae, diaphragmatic defects and distal limb deformities
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960102%2961%3A1%3C68%3A%3AAID-AJMG13%3E3.0.CO%3B2-U
retrieved
21 January 2018
Fryns syndrome: a variable MCA syndrome with diaphragmatic defects, coarse face, and distal limb hypoplasia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960102%2961%3A1%3C68%3A%3AAID-AJMG13%3E3.0.CO%3B2-U
retrieved
21 January 2018
Trisomy 22 with holoprosencephaly: a clinicopathologic study
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960102%2961%3A1%3C68%3A%3AAID-AJMG13%3E3.0.CO%3B2-U
retrieved
21 January 2018
Trisomy 22 with congenital diaphragmatic hernia and absence of corpus callosum in a liveborn premature infant
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960102%2961%3A1%3C68%3A%3AAID-AJMG13%3E3.0.CO%3B2-U
retrieved
21 January 2018
Trisomy 22 and facioauriculovertebral (Goldenhar) sequence
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960102%2961%3A1%3C68%3A%3AAID-AJMG13%3E3.0.CO%3B2-U
retrieved
21 January 2018
Terminal deletion of 6q and Fryns syndrome: a microdeletion/syndrome pair?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960102%2961%3A1%3C68%3A%3AAID-AJMG13%3E3.0.CO%3B2-U
retrieved
21 January 2018
Trisomy 22: no longer an enigma
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960102%2961%3A1%3C68%3A%3AAID-AJMG13%3E3.0.CO%3B2-U
retrieved
21 January 2018
Fryns syndrome: a new variable multiple congenital anomaly (MCA) syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960102%2961%3A1%3C68%3A%3AAID-AJMG13%3E3.0.CO%3B2-U
retrieved
21 January 2018
Trisomy 22 in a liveborn infant with multiple congenital anomalies
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960102%2961%3A1%3C68%3A%3AAID-AJMG13%3E3.0.CO%3B2-U
retrieved
21 January 2018
Pallister-Killian and Fryns syndromes: nosology
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960102%2961%3A1%3C68%3A%3AAID-AJMG13%3E3.0.CO%3B2-U
retrieved
21 January 2018
The syndrome of diaphragmatic hernia, abnormal face and distal limb anomalies (Fryns syndrome): report of two sibs with further delineation of this multiple congenital anomaly (MCA) syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960102%2961%3A1%3C68%3A%3AAID-AJMG13%3E3.0.CO%3B2-U
retrieved
21 January 2018
Two live-born infants with trisomy 22.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960102%2961%3A1%3C68%3A%3AAID-AJMG13%3E3.0.CO%3B2-U
retrieved
21 January 2018
Quinacrine fluorescence and Giemsa banding in trisomy 22
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960102%2961%3A1%3C68%3A%3AAID-AJMG13%3E3.0.CO%3B2-U
retrieved
21 January 2018
Fryns syndrome: a predictable, lethal pattern of multiple congenital anomalies
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960102%2961%3A1%3C68%3A%3AAID-AJMG13%3E3.0.CO%3B2-U
retrieved
21 January 2018
Incomplete trisomy 22. III. Mosaic-trisomy 22 and the problem of full trisomy 22
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960102%2961%3A1%3C68%3A%3AAID-AJMG13%3E3.0.CO%3B2-U
retrieved
21 January 2018
Fryns syndrome in a girl born to consanguineous parents
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960102%2961%3A1%3C68%3A%3AAID-AJMG13%3E3.0.CO%3B2-U
retrieved
21 January 2018
Trisomy 22 confirmed by fluorescent in situ hybridization
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960102%2961%3A1%3C68%3A%3AAID-AJMG13%3E3.0.CO%3B2-U
retrieved
21 January 2018
Fryns syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960102%2961%3A1%3C68%3A%3AAID-AJMG13%3E3.0.CO%3B2-U
retrieved
21 January 2018
Apparently nonmosaic trisomy 22: clinical report and review
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960102%2961%3A1%3C68%3A%3AAID-AJMG13%3E3.0.CO%3B2-U
retrieved
21 January 2018
Trisomy 22 in a newborn with multiple malformations
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960102%2961%3A1%3C68%3A%3AAID-AJMG13%3E3.0.CO%3B2-U
retrieved
21 January 2018
Identifiers
DOI
10.1002/(SICI)1096-8628(19960102)61:1<68::AID-AJMG13>3.0.CO;2-U
0 references
PubMed publication ID
8741922
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8741922
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8741922%20AND%20SRC:MED&resulttype=core&format=json
retrieved
18 October 2019
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