(Q56269958)

English

The mutation ROR2W749X, linked to human BDB, is a recessive mutation in the mouse, causing brachydactyly, mediating patterning of joints and modeling recessive Robinow syndrome

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scholarly article

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Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18353862%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

The mutation ROR2W749X, linked to human BDB, is a recessive mutation in the mouse, causing brachydactyly, mediating patterning of joints and modeling recessive Robinow syndrome (English)

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18353862%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

Robinow syndrome

1 reference

based on heuristic

inferred from title

Sigmar Stricker

2

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18353862%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

Aris Economides

17

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4 January 2020

15

object named as

Stefan Mundlos

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4 January 2020

5

object named as

Florian Witte

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4 January 2020

author name string

Regina Raz

1

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4 January 2020

Elizabetta Gazzerro

3

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4 January 2020

Julie L Clor

4

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4 January 2020

Harakiran Nistala

6

1 reference

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4 January 2020

Stefanie Zabski

7

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4 January 2020

Renata C Pereira

8

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4 January 2020

Lisa Stadmeyer

9

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4 January 2020

Xiangmin Wang

10

1 reference

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4 January 2020

Lori Gowen

11

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4 January 2020

Mark W Sleeman

12

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4 January 2020

George D Yancopoulos

13

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4 January 2020

Ernesto Canalis

14

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4 January 2020

David M Valenzuela

16

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4 January 2020

language of work or name

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publication date

19 March 2008

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4 January 2020

number of pages

11

1 reference

based on heuristic

inferred from page(s)

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4 January 2020

135

1 reference

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4 January 2020

9

1 reference

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4 January 2020

1713-1723

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4 January 2020

High-throughput engineering of the mouse genome coupled with high-resolution expression analysis

1 reference

5 June 2022

https://opencitations.net/index/coci/api/v1/citations/10.1038/NBT822

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