X-chromosomal maternal and fetal SNPs and the risk of spontaneous preterm delivery in a Danish/Norwegian genome-wide association study (Q34685114)

3 August 2017

title

X-chromosomal maternal and fetal SNPs and the risk of spontaneous preterm delivery in a Danish/Norwegian genome-wide association study (English)

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genome-wide association study

3 August 2017

main subject

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14

Mads Melbye

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Bjarke Feenstra

object named as

Bjarke Feenstra

4

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Frank Geller

object named as

Frank Geller

11

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Håkon K. Gjessing

13

object named as

Håkon K Gjessing

1 reference

3 August 2017

12

Per Magnus

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3 August 2017

8

Nils-Halvdan Morken

1 reference

3 August 2017

15

Bo Jacobsson

1 reference

3 August 2017

Solveig Myking

1

1 reference

3 August 2017

Heather A Boyd

2

1 reference

3 August 2017

Ronny Myhre

3

1 reference

3 August 2017

Astanand Jugessur

5

1 reference

3 August 2017

Aase S Devold Pay

6

1 reference

3 August 2017

Ingrid H G Ostensen

7

1 reference

3 August 2017

Tamara Busch

9

1 reference

3 August 2017

Kelli K Ryckman

10

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3 August 2017

Jeffrey C Murray

16

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3 August 2017

language of work or name

English

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publication date

16 April 2013

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3 August 2017

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3 August 2017

volume

8

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3 August 2017

issue

4

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3 August 2017

page(s)

e61781

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Creative Commons Attribution 4.0 International

3 August 2017

copyright license

start time

16 April 2013

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

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describes a project that uses

genome-wide association study

1 reference

X-linked genes and risk of orofacial clefts: evidence from two population-based studies in Scandinavia

inferred from title

cites work

1 reference

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7 July 2018

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Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus

7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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Identifiers

DOI

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3 August 2017

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3 August 2017

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