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English
Head development. Craniofacial genetics makes headway.
scientific article published on April 1995
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
7627544
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7627544%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 October 2019
review article
1 reference
stated in
Europe PubMed Central
title
Head development. Craniofacial genetics makes headway
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
7627544
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7627544%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 October 2019
author
Joy M. Richman
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
7627544
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7627544%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 October 2019
author name string
Richman JM
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
7627544
retrieved
20 September 2017
language of work or name
English
0 references
publication date
1 April 1995
1 reference
stated in
Europe PubMed Central
PubMed ID
7627544
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7627544%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 October 2019
published in
Current Biology
1 reference
stated in
Europe PubMed Central
PubMed ID
7627544
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7627544%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 October 2019
volume
5
1 reference
stated in
Europe PubMed Central
PubMed ID
7627544
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7627544%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 October 2019
issue
4
1 reference
stated in
Europe PubMed Central
PubMed ID
7627544
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7627544%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 October 2019
page(s)
345-348
1 reference
stated in
Europe PubMed Central
PubMed ID
7627544
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7627544%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 October 2019
cites work
The role of the neural crest in patterning of avian cranial skeletal, connective, and muscle tissues
1 reference
stated in
Crossref
reference URL
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retrieved
7 January 2021
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Neural crest cell formation and migration in the developing embryo
1 reference
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reference URL
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7 January 2021
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The signalling molecule BMP4 mediates apoptosis in the rhombencephalic neural crest
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-9822%2895%2900068-6
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7 January 2021
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High postnatal lethality and testis degeneration in retinoic acid receptor alpha mutant mice
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-9822%2895%2900068-6
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
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-9822%2895%2900068-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Jackson-Weiss and Crouzon syndromes are allelic with mutations in fibroblast growth factor receptor 2
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-9822%2895%2900068-6
retrieved
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
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https://api.crossref.org/works/10.1016%2FS0960-9822%2895%2900068-6
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7 January 2021
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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%2FS0960-9822%2895%2900068-6
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%2FS0960-9822%2895%2900068-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
FGF-2: apical ectodermal ridge growth signal for chick limb development
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-9822%2895%2900068-6
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7 January 2021
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inferred from DOI database lookup
FGF-4 replaces the apical ectodermal ridge and directs outgrowth and patterning of the limb
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-9822%2895%2900068-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in the gene encoding fibroblast growth factor receptor-3 in achondroplasia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-9822%2895%2900068-6
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
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-9822%2895%2900068-6
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7 January 2021
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A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosis
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-9822%2895%2900068-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0960-9822(95)00068-6
1 reference
stated in
Europe PubMed Central
PubMed ID
7627544
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7627544%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 October 2019
PubMed ID
7627544
1 reference
stated in
Europe PubMed Central
PubMed ID
7627544
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7627544%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 October 2019
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