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
Crossref DOI link: https://doi.org/10.1007/s12041-015-0578-x
Published Online: 2015-11-18
Published Print: 2015-12
Update policy: https://doi.org/10.1007/springer_crossmark_policy
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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