A familial GLI2 deletion (2q14.2) not associated with the holoprosencephaly syndrome phenotype

Publisher： John Wiley & Sons Inc

E-ISSN： 1552-4833|167|5|1121-1124

ISSN： 1552-4825

Source： American Journal Of Medical Genetics Part A, Vol.167, Iss.5, 2015-05, pp. : 1121-1124

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