Publications
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Filters: Keyword is Molecular Sequence Data and Author is Pfundt, Rolph [Clear All Filters]
NR2F1 mutations cause optic atrophy with intellectual disability. Am J Hum Genet. 2014 ;94(2):303-9.
. Absence of heterozygosity due to template switching during replicative rearrangements. Am J Hum Genet. 2015 ;96(4):555-64.
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