Recurrent 200-kb deletions of 16p11.2 that include the SH2B1 gene are associated with developmental delay and obesity. (Q50302372)

2 March 2018

title

Recurrent 200-kb deletions of 16p11.2 that include the SH2B1 gene are associated with developmental delay and obesity. (English)

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2 March 2018

Ruxandra Bachmann-Gagescu

main subject

obesity

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author

1

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Aline I. Hamati

8

Aline Hamati

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Heather C. Mefford

2

Heather C Mefford

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Evan E. Eichler

14

Evan E Eichler

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Gwen M Glew

4

Gwen M Glew

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Patricia I Bader

7

Patricia I Bader

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Anne V Hing

5

Anne V Hing

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Hiltrud Muhle

12

Hiltrud Muhle

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Blake C Ballif

15

Blake C Ballif

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author name string

Charles Cowan

3

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Stephanie Wallace

6

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Pamela J Reitnauer

9

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Rosemarie Smith

10

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David W Stockton

11

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Ingo Helbig

13

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Jill Rosenfeld

16

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Karen D Tsuchiya

17

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language of work or name

English

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publication date

1 October 2010

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2 March 2018

published in

Genetics in Medicine

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2 March 2018

volume

12

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2 March 2018

page(s)

641-647

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issue

10

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https://scigraph.springernature.com/pub.10.1097/gim.0b013e3181ef4286

exact match

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cites work

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Microdeletion encompassing MAPT at chromosome 17q21.3 is associated with developmental delay and learning disability

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21 January 2018

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A new highly penetrant form of obesity due to deletions on chromosome 16p11.2.

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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10.1097/GIM.0B013E3181EF4286

21 January 2018

Identifiers

DOI

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2 March 2018

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1 reference

2 March 2018