Assessing structural variation in a personal genome-towards a human reference diploid genome. (Q35607005)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25886820%20AND%20SRC:MED&resulttype=core&format=json

5 March 2020

title

Assessing structural variation in a personal genome-towards a human reference diploid genome (English)

1 reference

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5 March 2020

author

Claudia Gonzaga-Jauregui

4

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5 March 2020

Caleb F Davis

8

1 reference

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5 March 2020

Simon White

17

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5 March 2020

Feng Zhang

21

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5 March 2020

Kim C Worley

28

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5 March 2020

29

James R Lupski

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5 March 2020

31

Richard A Gibbs

1 reference

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5 March 2020

25

Donna M Muzny

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5 March 2020

22

Pawel Stankiewicz

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5 March 2020

23

David A Wheeler

1 reference

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5 March 2020

6

Deborah I Ritter

1 reference

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5 March 2020

9

Mahmoud Dahdouli

1 reference

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5 March 2020

30

Eric Boerwinkle

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5 March 2020

author name string

Adam C English

1

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5 March 2020

William J Salerno

2

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5 March 2020

Oliver A Hampton

3

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5 March 2020

Shruthi Ambreth

5

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5 March 2020

Christine R Beck

7

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5 March 2020

Singer Ma

10

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5 March 2020

Andrew Carroll

11

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5 March 2020

Narayanan Veeraraghavan

12

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5 March 2020

Jeremy Bruestle

13

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5 March 2020

Becky Drees

14

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5 March 2020

Alex Hastie

15

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5 March 2020

Ernest T Lam

16

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5 March 2020

Pamela Mishra

18

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5 March 2020

Min Wang

19

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5 March 2020

Yi Han

20

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5 March 2020

Jeffrey G Reid

24

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5 March 2020

Jeffrey Rogers

26

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5 March 2020

Aniko Sabo

27

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5 March 2020

language of work or name

English

0 references

publication date

11 April 2015

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5 March 2020

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5 March 2020

volume

16

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5 March 2020

page(s)

286

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Creative Commons Attribution 4.0 International

5 March 2020

copyright license

start time

11 April 2015

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

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27 July 2018

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25 September 2018

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25 September 2018

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25 September 2018

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25 September 2018

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25 September 2018

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Phenotypic consequences of genetic variation at hemizygous alleles: Sotos syndrome is a contiguous gene syndrome incorporating coagulation factor twelve (FXII) deficiency

25 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/25886820

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1186/S12864-015-1479-3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25886820%20AND%20SRC:MED&resulttype=core&format=json

5 March 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25886820%20AND%20SRC:MED&resulttype=core&format=json

5 March 2020

1 reference

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