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Lim, E.C.P.
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Lim, E.C.P.
Showing
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Lim, E.C.P.
'
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1
An additional case of the recurrent 15q24.1 microdeletion syndrome and review of the literature
由
Ng, I.S.L.
,
Chin, W.-H.
,
Lim
,
E.C.P
.
,
Tan, E.-C.
出版 2014
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2
Gender-specific association of insertion/deletion polymorphisms in the nogo gene and chronic schizophrenia
由
Tan, E.-C.
,
Chong, S.-A.
,
Wang, H.
,
Lim
,
E.C
.-
P
.
,
Teo, Y.-Y.
出版 2014
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3
Ethnicity and OPRM variant independently predict pain perception and patient-controlled analgesia usage for post-operative pain
由
Tan, E.-C.
,
Lim
,
E.C.P
.
,
Teo, Y.-Y.
,
Lim, Y.
,
Law, H.-Y.
,
Sia, A.T.
出版 2014
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4
Chromosome 15q11-q13 copy number gain detected by array-CGH in two cases with a maternal methylation pattern
由
Tan, E.-S
,
Yong, M.-H
,
Lim
,
E.C.P
,
Li, Z.-H
,
Brett, M.S.Y
,
Tan, E.-C
出版 2020
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5
De novo trisomy 12p in twin girls with different levels of mosaicism
由
Lim
,
E.C.P
.
,
Ng, I.S.L.
,
Yong, M.-H.
,
Yon, H.-Y.
,
Brett, M.S.Y.
,
Tan, E.-C.
出版 2014
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6
A submicroscopic deletion involving part of the CREBBP gene detected by array-CGH in a patient with Rubinstein-Taybi syndrome
由
Lai, A.H.M.
,
Brett, M.S.
,
Chin, W.-H.
,
Lim
,
E.C.P
.
,
Ng, J.S.H.
,
Tan, E.-C.
出版 2014
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7
De novo 3q22.1 q24 deletion associated with multiple congenital anomalies, growth retardation and intellectual disability
由
Brett, M.S.
,
Ng, I.S.L.
,
Lim
,
E.C.P
.
,
Yong, M.H.
,
Li, Z.
,
Lai, A.
,
Tan, E.-C.
出版 2014
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8
A118G single nucleotide polymorphism of human μ-opioid receptor gene influences pain perception and patient-controlled intravenous morphine consumption after intrathecal morphine f...
由
Sia, A.T.
,
Goh, R.W.C.
,
Law, H.Y.
,
Landau, R.
,
Teo, Y.-Y.
,
Tan, E.C.
,
Lim, Y.
,
Lim
,
E.C.P
.
出版 2011
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