Article
Whole exome sequencing reveals a MLL de novo mutation associated with mild developmental delay and without 'hairy elbows': expanding the phenotype of Wiedemann-Steiner syndrome.
Journal of genetics - 1 Dec 2015
Steel Dora, Salpietro Vincenzo, Phadke Rahul, Pitt Matthew, Gentile Giulia, Massoud Ahmed, Batten Leigh, Bashamboo Anu, Mcelreavey Ken, Saggar Anand, Kinali Maria
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