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Ullmann et al., 2007 - Google Patents

Array CGH identifies reciprocal 16p13. 1 duplications and deletions that predispose to autism and/or mental retardation

Ullmann et al., 2007

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Document ID
3831307051760838866
Author
Ullmann R
Turner G
Kirchhoff M
Chen W
Tonge B
Rosenberg C
Field M
Vianna‐Morgante A
Christie L
Krepischi‐Santos A
Banna L
Brereton A
Hill A
Bisgaard A
Müller I
Hultschig C
Erdogan F
Wieczorek G
Ropers H
Publication year
Publication venue
Human mutation

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Snippet

Autism and mental retardation (MR) are often associated, suggesting that these conditions are etiologically related. Recently, array‐based comparative genomic hybridization (array CGH) has identified submicroscopic deletions and duplications as a common cause of MR …
Continue reading at www.molgen.mpg.de (PDF) (other versions)

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