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Schwartzentruber, Jeremy
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Journal Article
Mirzaa G
,
Parry DA
,
Fry AE
,
Giamanco KA
,
Schwartzentruber J
,
Vanstone M
,
Logan CV
,
Roberts N
,
Johnson CA
,
Singh S
et al.
. 2014.
De novo CCND2 mutations leading to stabilization of cyclin D2 cause megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome.
.
Nat Genet. 46(5):510-515.