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A novel CBFA1 mutation (R190W) in an Italian family with cleidocranial dysplasia
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instance of
scholarly article
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title
A novel CBFA1 mutation (R190W) in an Italian family with cleidocranial dysplasia
(English)
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main subject
cleidocranial dysplasia
1 reference
based on heuristic
inferred from title
author
Filippo Maria Santorelli
series ordinal
8
object named as
Filippo M. Santorelli
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author name string
Aldo Giannotti
series ordinal
1
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Alessandra Tessa
series ordinal
2
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Clarice Patrono
series ordinal
3
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Lucia De Florio
series ordinal
4
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Margherita Velardo
series ordinal
5
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Carlo Dionisi-Vici
series ordinal
6
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Enrico Bertini
series ordinal
7
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language of work or name
English
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publication date
2000
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published in
Human Mutation
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volume
16
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issue
3
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page(s)
277-277
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Identifiers
DOI
10.1002/1098-1004(200009)16:3<277::AID-HUMU25>3.0.CO;2-V
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PubMed publication ID
10980549
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