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Simmer, J.P
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Simmer, J.P
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Simmer, J.P
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Hypoplastic AI with Highly Variable Expressivity Caused by ENAM Mutations
by
Hu, J.C.C
,
Hyun, H.K
,
Kang, J.
,
Kasimoglu, Y.
,
Kim, J.W
,
Kim, Y.J
,
Kim, Y.J
,
Koruyucu, M.
,
Lee, S.H
,
Lee, Z.H
,
Seymen, F.
,
Shin, T.J
,
Simmer
,
J.P
Published 2018
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Related Subjects
Amelogenesis Imperfecta
Child
Consanguinity
ENAM protein, human
Extracellular Matrix Proteins
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Humans
Mutation
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Polymerase Chain Reaction
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Whole Exome Sequencing
Young Adult
amelogenesis imperfecta
case report
child
consanguinity
enamel
enamelin
female
genetics
human
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phenotype
polymerase chain reaction
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