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English
Mutations in FGFR1 and FGFR2 cause familial and sporadic Pfeiffer syndrome
scientific article
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Statements
instance of
scholarly article
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title
Mutations in FGFR1 and FGFR2 cause familial and sporadic Pfeiffer syndrome
(English)
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main subject
Pfeiffer syndrome
1 reference
based on heuristic
inferred from title
author name string
U Schell
series ordinal
1
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A Hehr
series ordinal
2
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G J Feldman
series ordinal
3
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N H Robin
series ordinal
4
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E H Zackai
series ordinal
5
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C de Die-Smulders
series ordinal
6
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D H Viskochil
series ordinal
7
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J M Stewart
series ordinal
8
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G Wolff
series ordinal
9
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H Ohashi
series ordinal
10
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language of work or name
English
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publication date
March 1995
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published in
Human Molecular Genetics
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volume
4
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page(s)
323-8
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issue
3
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Identifiers
DOI
10.1093/HMG/4.3.323
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1744814
OpenCitations bibliographic resource ID
1744814
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1744814
PubMed ID
7795583
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1744814
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