Genomic screening of fibroblast growth-factor receptor 2 reveals a wide spectrum of mutations in patients with syndromic craniosynostosis (Q28344714)

Andrew O M Wilkie

15

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Maximilian Muenke

Maximilian Muenke

14

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Alain Verloes

8

Alain Verloes

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Donna M McDonald-McGinn

11

Donna M McDonald-McGinn

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author name string

Shih-hsin Kan

1

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Navaratnam Elanko

2

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David Johnson

3

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Laura Cornejo-Roldan

4

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Jackie Cook

5

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Elsa W Reich

6

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Susan Tomkins

7

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Stephen R F Twigg

9

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Sahan Rannan-Eliya

10

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Elaine H Zackai

12

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Steven A Wall

American Journal of Human Genetics

13

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language of work or name

English

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publication date

February 2002

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published in

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volume

70

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issue

2

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page(s)

472-86

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cites work

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PubMed

https://pubmed.ncbi.nlm.nih.gov/11781872

12 December 2020

inferred from PubMed ID database lookup

KinMutBase, a database of human disease-causing protein kinase mutations

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/11781872

12 December 2020

inferred from PubMed ID database lookup

Epidermal mosaicism producing localised acne: somatic mutation in FGFR2

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Identifiers

DOI

10.1086/338758

1 reference

release_pq3gv774x5ajzml4b5ocu6y2nm

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/pq3gv774x5ajzml4b5ocu6y2nm

24 November 2022

mapped directly with Wikidata item

1 reference

1 reference

PubMed publication ID

11781872

1 reference