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Novel homozygous ALX4 mutation causing frontonasal dysplasia‐2 in a patient with meningoencephalocele
Author(s) -
Meloni V.A.,
MoysésOliveira M.,
Melo M.C.C.,
Caneloi T.P.,
Dantas A.G.,
Soares M.F.F.,
Fock R.,
Rodrigues de Nicola P.D.,
DiasdaSilva M.R.,
Melaragno M.I.
Publication year - 2015
Publication title -
clinical genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.543
H-Index - 102
eISSN - 1399-0004
pISSN - 0009-9163
DOI - 10.1111/cge.12595
Subject(s) - medical genetics , developmental genetics , genetics , medicine , biology , regulation of gene expression , gene
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