Associated Papers
Skewed X-inactivation in a family with DLG3-associated X-linked intellectual disability.
Gieldon L et al.
American Journal of Medical Genetics. Part A, 2017
X-exome sequencing in Finnish families with intellectual disability--four novel mutations and two novel syndromic phenotypes.
Philips AK et al.
Orphanet Journal of Rare Diseases, 2014
[Exome sequencing revealed Allan-Herndon-Dudley syndrome underlying multiple disabilities].
Arvio M et al.
Duodecim; Laaketieteellinen Aikakauskirja, 2014
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