PBX1 haploinsufficiency leads to syndromic congenital anomalies of the kidney and urinary tract (CAKUT) in humans (Q42428334)

31 October 2017

PBX1 haploinsufficiency leads to syndromic congenital anomalies of the kidney and urinary tract (CAKUT) in humans (English)

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31 October 2017

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GOA release 2020-03-11

author

Pierre F Ray

6

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31 May 2020

Véronique Satre

4

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31 May 2020

Antonio Novelli

14

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31 May 2020

Ida Vogel

19

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31 May 2020

Charles Coutton

30

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31 May 2020

9

Sylvie Jaillard

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31 May 2020

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Pauline Le Tanno

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31 May 2020

27

Pierre-Simon Jouk

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31 May 2020

3

Marie Bidart

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31 May 2020

5

Radu Harbuz

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31 May 2020

23

Florence Amblard

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31 May 2020

7

Caroline Bosson

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31 May 2020

8

Klaus Dieterich

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31 May 2020

29

Hervé Sartelet

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31 May 2020

author name string

Julie Breton

2

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31 May 2020

Sylvie Odent

10

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31 May 2020

Gemma Poke

11

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31 May 2020

Rachel Beddow

12

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31 May 2020

Maria Christina Digilio

13

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31 May 2020

Laura Bernardini

15

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31 May 2020

Maria Antonietta Pisanti

16

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31 May 2020

Luisa Mackenroth

17

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31 May 2020

Karl Hackmann

18

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31 May 2020

Rikke Christensen

20

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31 May 2020

Siv Fokstuen

21

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31 May 2020

Frédérique Béna

22

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31 May 2020

Francoise Devillard

24

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31 May 2020

Gaelle Vieville

25

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31 May 2020

Alexia Apostolou

26

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31 May 2020

Fitsum Guebre-Egziabher

28

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31 May 2020

language of work or name

English

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publication date

7 March 2017

1 reference

Journal of Medical Genetics

31 October 2017

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31 May 2020

volume

54

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31 May 2020

page(s)

502-510

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31 May 2020

issue

7

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10.1136/JMEDGENET-2016-104435

31 May 2020

Identifiers

DOI

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release_ebam5vc3sbhivmkzzdlgz56a6m

31 May 2020

Fatcat ID

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Fatcat

https://api.fatcat.wiki/v0/release/ebam5vc3sbhivmkzzdlgz56a6m

mapped directly with Wikidata item

24 November 2022

based on heuristic

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