Brachydactyly type A2 associated with a defect in proGDF5 processing (Q46802209)

25 December 2017

title

Brachydactyly type A2 associated with a defect in proGDF5 processing (English)

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25 December 2017

main subject

brachydactyly type A2

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Petra Seemann

2

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Stefan Mundlos

8

object named as

Stefan Mundlos

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25 December 2017

author name string

Frank Plöger

1

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25 December 2017

Mareen Schmidt-von Kegler

3

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25 December 2017

Katarina Lehmann

4

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25 December 2017

Jörg Seidel

5

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Klaus W Kjaer

6

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Jens Pohl

7

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publication date

18 January 2008

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25 December 2017

published in

Human Molecular Genetics

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25 December 2017

volume

17

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25 December 2017

issue

9

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25 December 2017

page(s)

1222-1233

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25 December 2017

Multiple joint and skeletal patterning defects caused by single and double mutations in the mouse Gdf6 and Gdf5 genes

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Activating and deactivating mutations in the receptor interaction site of GDF5 cause symphalangism or brachydactyly type A2

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

Identifiers

DOI

10.1093/HMG/DDN012

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25 December 2017

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25 December 2017