(Q40220391)

18 September 2017

A syndromic form of Pierre Robin sequence is caused by 5q23 deletions encompassing FBN2 and PHAX. (English)

1 reference

18 September 2017

8

1 reference

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1 June 2020

Isabel Hanson

4

1 reference

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1 June 2020

Felicity Mehendale

6

1 reference

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1 June 2020

Jeanne Amiel

7

1 reference

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1 June 2020

Antonio Percesepe

9

1 reference

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1 June 2020

Laura Mazzanti

10

1 reference

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1 June 2020

Karen Temple

14

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1 June 2020

David R. FitzPatrick

15

1 reference

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1 June 2020

5

Helen V Firth

1 reference

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1 June 2020

author name string

Morad Ansari

1

1 reference

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1 June 2020

Jacqueline K Rainger

2

1 reference

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1 June 2020

Jennie E Murray

3

1 reference

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1 June 2020

Alan Fryer

11

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1 June 2020

Paola Ferrari

12

1 reference

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1 June 2020

Koenraad Devriendt

13

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1 June 2020

publication date

3 September 2014

1 reference

European Journal of Medical Genetics

18 September 2017

1 reference

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1 June 2020

volume

57

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1 June 2020

issue

10

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1 June 2020

page(s)

587-595

1 reference