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Search Results - Reijnders, M.R.F.
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Okur‐Chung neurodevelopmental syndrome: Eight additional cases with implications on phenotype and genotype expansion
by
Chiu, A.T.G.
,
Pei, S.L.C.
,
Mak, C.C.Y.
,
Leung, G.K.C.
,
Yu, M.H.C.
,
Lee, S.L.
,
Vreeburg, M.
,
Pfundt, R.
,
van der Burgt, I.
,
Kleefstra, T.
,
Frederic, T.M.‐T.
,
Nambot, S.
,
Faivre, L.
,
Bruel, A.‐L.
,
Rossi, M.
,
Isidor, B.
,
Küry, S.
,
Cogne, B.
,
Besnard, T.
,
Willems, M.
,
Reijnders, M.R.F.
,
Chung, B.H.Y.
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Clinical genetics
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Clinical Genetics
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Casein Kinase Ii - Chemistry
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Child
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Csnk2A1
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Developmental Delay
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