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Fibroblast growth factors, their receptors and receptor disorders
scientific article published on April 1997
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scholarly article
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Europe PubMed Central
PubMed ID
9174888
retrieved
1 October 2017
review article
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Europe PubMed Central
title
Fibroblast growth factors, their receptors and receptor disorders
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
9174888
retrieved
1 October 2017
author name string
Gorlin RJ
series ordinal
1
1 reference
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Europe PubMed Central
PubMed ID
9174888
retrieved
1 October 2017
publication date
1 April 1997
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Europe PubMed Central
PubMed ID
9174888
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1 October 2017
published in
Journal of Cranio-Maxillofacial Surgery
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stated in
Europe PubMed Central
PubMed ID
9174888
retrieved
1 October 2017
volume
25
1 reference
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Europe PubMed Central
PubMed ID
9174888
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1 October 2017
issue
2
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Europe PubMed Central
PubMed ID
9174888
retrieved
1 October 2017
page(s)
69-79
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Europe PubMed Central
PubMed ID
9174888
retrieved
1 October 2017
cites work
Jackson-Weiss syndrome: clinical and radiological findings in a large kindred and exclusion of the gene from 7p21 and 5qter
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1010-5182%2897%2980048-0
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7 January 2021
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A severe case of Beare-Stevenson syndrome and associated congenital deformities
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reference URL
https://api.crossref.org/works/10.1016%2FS1010-5182%2897%2980048-0
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Effective indirect pulp capping (Cp-treatment)
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7 January 2021
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Progressive bony dysplasia in Apert syndrome
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https://api.crossref.org/works/10.1016%2FS1010-5182%2897%2980048-0
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7 January 2021
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A recurrent mutation in the tyrosine kinase domain of fibroblast growth factor receptor 3 causes hypochondroplasia
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1010-5182%2897%2980048-0
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7 January 2021
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Identical mutations in three different fibroblast growth factor receptor genes in autosomal dominant craniosynostosis syndromes
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reference URL
https://api.crossref.org/works/10.1016%2FS1010-5182%2897%2980048-0
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7 January 2021
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Craniosynostoses: phenotypic/molecular correlations
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reference URL
https://api.crossref.org/works/10.1016%2FS1010-5182%2897%2980048-0
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7 January 2021
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Birth prevalence studies of the Crouzon syndrome: comparison of direct and indirect methods
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https://api.crossref.org/works/10.1016%2FS1010-5182%2897%2980048-0
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7 January 2021
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Birth prevalence study of the Apert syndrome
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reference URL
https://api.crossref.org/works/10.1016%2FS1010-5182%2897%2980048-0
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7 January 2021
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Transforming growth factor beta s and fibroblast growth factors and their receptors: role in sutural biology and craniosynostosis
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1010-5182%2897%2980048-0
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7 January 2021
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Skeletal overgrowth and deafness in mice lacking fibroblast growth factor receptor 3.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1010-5182%2897%2980048-0
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7 January 2021
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Thanatophoric dysplasia in monozygotic twins discordant for cloverleaf skull: Prenatal diagnosis, clinical and pathological findings
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1010-5182%2897%2980048-0
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7 January 2021
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A Crouzon syndrome synonymous mutation activates a 5' splice site within the IIIc exon of the FGFR2 gene
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1010-5182%2897%2980048-0
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7 January 2021
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inferred from DOI database lookup
Crouzon disease with acanthosis nigricans and melanocytic nevi
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1010-5182%2897%2980048-0
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7 January 2021
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Crouzon syndrome: mutations in two spliceoforms of FGFR2 and a common point mutation shared with Jackson-Weiss syndrome
1 reference
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reference URL
https://api.crossref.org/works/10.1016%2FS1010-5182%2897%2980048-0
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7 January 2021
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Hypochondroplasia: Clinical and Radiological Aspects in 39 cases
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1010-5182%2897%2980048-0
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7 January 2021
based on heuristic
inferred from DOI database lookup
Beare-Stevenson cutis gyrata syndrome
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1010-5182%2897%2980048-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Localization of craniosynostosis Adelaide type to 4p16.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1010-5182%2897%2980048-0
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7 January 2021
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inferred from DOI database lookup
Jackson-Weiss and Crouzon syndromes are allelic with mutations in fibroblast growth factor receptor 2
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1010-5182%2897%2980048-0
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7 January 2021
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inferred from DOI database lookup
Craniosynostosis, midfacial hypoplasia, and foot abnormalities: An autosomal dominant phenotype in a large Amish kindred
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1010-5182%2897%2980048-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
An association of acanthosis nigricans and Crouzon syndrome
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1010-5182%2897%2980048-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cloverleaf skull associated with Pfeiffer syndrome: pathology and management.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1010-5182%2897%2980048-0
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7 January 2021
based on heuristic
inferred from DOI database lookup
FGFR2 mutations in Pfeiffer syndrome
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1010-5182%2897%2980048-0
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7 January 2021
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inferred from DOI database lookup
Achondroplasia
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1010-5182%2897%2980048-0
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7 January 2021
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inferred from DOI database lookup
Thanatophoric dwarfism. A condition confused with achondroplasia in the neonate, with brief comments on achondrogenesis and homozygous achondroplasia
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1010-5182%2897%2980048-0
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7 January 2021
based on heuristic
inferred from DOI database lookup
A gene for achondroplasia–hypochondroplasia maps to chromosome 4p
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1010-5182%2897%2980048-0
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7 January 2021
based on heuristic
inferred from DOI database lookup
Two craniosynostotic syndrome loci, Crouzon and Jackson-Weiss, map to chromosome 10q23-q26
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1010-5182%2897%2980048-0
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7 January 2021
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Effect on splicing of a silent FGFR2 mutation in Crouzon syndrome
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1010-5182%2897%2980048-0
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7 January 2021
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inferred from DOI database lookup
Growth and development in thanatophoric dysplasia.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1010-5182%2897%2980048-0
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7 January 2021
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inferred from DOI database lookup
Fibroblast growth factor receptor 3 (FGFR3) transmembrane mutation in Crouzon syndrome with acanthosis nigricans
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1010-5182%2897%2980048-0
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7 January 2021
based on heuristic
inferred from DOI database lookup
Exclusive paternal origin of new mutations in Apert syndrome
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1010-5182%2897%2980048-0
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7 January 2021
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Spinal neurological complications of achondroplasia. Results of surgical treatment
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1010-5182%2897%2980048-0
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7 January 2021
based on heuristic
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Fibroblast-growth-factor receptor mutations in human skeletal disorders
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1010-5182%2897%2980048-0
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7 January 2021
based on heuristic
inferred from DOI database lookup
A common mutation in the fibroblast growth factor receptor 1 gene in Pfeiffer syndrome
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1010-5182%2897%2980048-0
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7 January 2021
based on heuristic
inferred from DOI database lookup
Graded activation of fibroblast growth factor receptor 3 by mutations causing achondroplasia and thanatophoric dysplasia
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1010-5182%2897%2980048-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in the third immunoglobulin domain of the fibroblast growth factor receptor-2 gene in Crouzon syndrome
1 reference
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reference URL
https://api.crossref.org/works/10.1016%2FS1010-5182%2897%2980048-0
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7 January 2021
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inferred from DOI database lookup
Novel FGFR2 mutations in Crouzon and Jackson-Weiss syndromes show allelic heterogeneity and phenotypic variability
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1010-5182%2897%2980048-0
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7 January 2021
based on heuristic
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A gene for Crouzon craniofacial dysostosis maps to the long arm of chromosome 10.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1010-5182%2897%2980048-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Fibroblast growth factor receptor 2 mutations in Beare-Stevenson cutis gyrata syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1010-5182%2897%2980048-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Spectrum of craniosynostosis phenotypes associated with novel mutations at the fibroblast growth factor receptor 2 locus
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1010-5182%2897%2980048-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in the fibroblast growth factor receptor 2 gene cause Crouzon syndrome
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1010-5182%2897%2980048-0
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7 January 2021
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An unusual association of acanthosis nigricans and Crouzon's disease--a case report
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1010-5182%2897%2980048-0
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7 January 2021
based on heuristic
inferred from DOI database lookup
Linkage of Pfeiffer syndrome to chromosome 8 centromere and evidence for genetic heterogeneity
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1010-5182%2897%2980048-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Clinical and genetic heterogeneity of hypochondroplasia
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1010-5182%2897%2980048-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identical mutations in the FGFR2 gene cause both Pfeiffer and Crouzon syndrome phenotypes
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1010-5182%2897%2980048-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Variable expression in Pfeiffer syndrome.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1010-5182%2897%2980048-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in FGFR1 and FGFR2 cause familial and sporadic Pfeiffer syndrome
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1010-5182%2897%2980048-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in the transmembrane domain of FGFR3 cause the most common genetic form of dwarfism, achondroplasia
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1010-5182%2897%2980048-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Achondroplasia-hypochondroplasia complex
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1010-5182%2897%2980048-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Predisposition for cysteine substitutions in the immunoglobulin-like chain of FGFR2 in Crouzon syndrome
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1010-5182%2897%2980048-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cutis gyratum and acanthosis nigricans associated with other anomalies: a distinctive syndrome
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1010-5182%2897%2980048-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A glycine 375-to-cysteine substitution in the transmembrane domain of the fibroblast growth factor receptor-3 in a newborn with achondroplasia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1010-5182%2897%2980048-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Thanatophoric dysplasia (types I and II) caused by distinct mutations in fibroblast growth factor receptor 3.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1010-5182%2897%2980048-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A gene encoding a fibroblast growth factor receptor isolated from the Huntington disease gene region of human chromosome 4.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1010-5182%2897%2980048-0
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7 January 2021
based on heuristic
inferred from DOI database lookup
Pfeiffer's type of acrocephalosyndactyly in two families.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1010-5182%2897%2980048-0
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7 January 2021
based on heuristic
inferred from DOI database lookup
Craniosynostosis suggestive of Saethre-Chotzen syndrome: clinical description of a large kindred and exclusion of candidate regions on 7p
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1010-5182%2897%2980048-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The gene for achondroplasia maps to the telomeric region of chromosome 4p
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1010-5182%2897%2980048-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Constitutive activation of fibroblast growth factor receptor 3 by the transmembrane domain point mutation found in achondroplasia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1010-5182%2897%2980048-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A recurrent mutation, ala391glu, in the transmembrane region of FGFR3 causes Crouzon syndrome and acanthosis nigricans
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1010-5182%2897%2980048-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1010-5182%2897%2980048-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Thanatophoric Dwarfism and Cloverleaf Skull (“Kleeblattschädel”)
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1010-5182%2897%2980048-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S1010-5182(97)80048-0
1 reference
stated in
Europe PubMed Central
PubMed ID
9174888
retrieved
1 October 2017
PubMed ID
9174888
1 reference
stated in
Europe PubMed Central
PubMed ID
9174888
retrieved
1 October 2017
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