Publications
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Filters: Author is Cheung, Yee Him and Keyword is Amino Acid Sequence [Clear All Filters]
A recurrent PDGFRB mutation causes familial infantile myofibromatosis. Am J Hum Genet 92, 996-1000 (2013).
Whole exome sequencing identifies de novo mutations in GATA6 associated with congenital diaphragmatic hernia. J Med Genet 51, 197-202 (2014).