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Singapore Medical Journal
|
October 20, 2011
Familial complex chromosomal rearrangement in a dysmorphic child with global developmental delay
C F Ngim, W T Keng, R Ariffin
Journal of Genetics
|
August 24, 2013
A mother with variant Turner syndrome and two daughters with trisomy X: a case report
S Ramachandram, W T Keng, R Ariffin, et al.
BMJ Case Reports
|
June 21, 2012
Rapid-onset obesity with hypothalamic dysfunction, hypoventilation and autonomic dysregulation (ROHHAD): a case with additional features and review of the literature
H B Chew, L H Ngu, W T Keng
Developmental Medicine and Child Neurology
|
October 1, 2003
A3243G mitochondrial mutation associated with polymicrogyria
W T Keng, D T Pilz, B Minns, et al.
Clinical Dysmorphology
|
October 29, 2002
Food aversion and facial dysmorphism--a newly described syndrome?
W T Keng, T Cole, D Pilz, et al.
Singapore Medical Journal
|
April 30, 2010
Mowat-Wilson syndrome: the first two Malaysian cases
S Balasubramaniam, W T Keng, L H Ngu, et al.
American Journal of Medical Genetics. Part A
|
April 6, 2006
A balanced reciprocal translocation in a case of hypomelanosis of Ito with confirmation of mosaicism using buccal cell interphase FISH
W T Keng, L Harewood, E Grace, et al.
The Malaysian Journal of Pathology
|
September 4, 2017
Molecular analysis of fragile X syndrome (FXS) among Malaysian patients with developmental disability
E Z Ali, Y Yakob, N Md Desa, et al.
Molecular Syndromology
|
May 9, 2013
Evaluation of Clinical Manifestations in Patients with Severe Lymphedema with and without CCBE1 Mutations
M Alders, A Mendola, L Adès, et al.
Neurology
|
May 28, 2010
Clinical and biochemical features of aromatic L-amino acid decarboxylase deficiency
L Brun, L H Ngu, W T Keng, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 11) with videos related to
Sort By:
Page
of 2
Singapore Medical Journal
|
October 20, 2011
Familial complex chromosomal rearrangement in a dysmorphic child with global developmental delay
C F Ngim, W T Keng, R Ariffin
Journal of Genetics
|
August 24, 2013
A mother with variant Turner syndrome and two daughters with trisomy X: a case report
S Ramachandram, W T Keng, R Ariffin, et al.
BMJ Case Reports
|
June 21, 2012
Rapid-onset obesity with hypothalamic dysfunction, hypoventilation and autonomic dysregulation (ROHHAD): a case with additional features and review of the literature
H B Chew, L H Ngu, W T Keng
Developmental Medicine and Child Neurology
|
October 1, 2003
A3243G mitochondrial mutation associated with polymicrogyria
W T Keng, D T Pilz, B Minns, et al.
Clinical Dysmorphology
|
October 29, 2002
Food aversion and facial dysmorphism--a newly described syndrome?
W T Keng, T Cole, D Pilz, et al.
Singapore Medical Journal
|
April 30, 2010
Mowat-Wilson syndrome: the first two Malaysian cases
S Balasubramaniam, W T Keng, L H Ngu, et al.
American Journal of Medical Genetics. Part A
|
April 6, 2006
A balanced reciprocal translocation in a case of hypomelanosis of Ito with confirmation of mosaicism using buccal cell interphase FISH
W T Keng, L Harewood, E Grace, et al.
The Malaysian Journal of Pathology
|
September 4, 2017
Molecular analysis of fragile X syndrome (FXS) among Malaysian patients with developmental disability
E Z Ali, Y Yakob, N Md Desa, et al.
Molecular Syndromology
|
May 9, 2013
Evaluation of Clinical Manifestations in Patients with Severe Lymphedema with and without CCBE1 Mutations
M Alders, A Mendola, L Adès, et al.
Neurology
|
May 28, 2010
Clinical and biochemical features of aromatic L-amino acid decarboxylase deficiency
L Brun, L H Ngu, W T Keng, et al.
Page
of 2