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S C Chong

Showing results (11-20 of 20) with videos related to

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Neonatology|September 9, 2008
Successful treatment of multiple subdural empyemata caused by Mycoplasma hominis in a newbornJosephine S C Chong, Simon Y T Tseung, Hugh S Lam, et al.
Hong Kong Medical Journal = Xianggang Yi Xue Za Zhi|January 26, 2026
Third-trimester prenatal brain imaging for early diagnosis of glutaric aciduria type 1 in monochorionic diamniotic twinsI Y M Wah, Y Cao, N K L Wong, et al.
BMC Medical Ethics|November 2, 2022
The view of Hong Kong parents on secondary use of dried blood spots in newborn screening programL L Hui, E A S Nelson, H B Deng, et al.
Prenatal Diagnosis|December 5, 2009
Noninvasive prenatal exclusion of haemoglobin Bart's using foetal DNA from maternal plasmaSherry S Y Ho, Samuel S C Chong, Evelyn S C Koay, et al.
Frontiers in Genetics|May 2, 2022
Investigation of Chromosomal Structural Abnormalities in Patients With Undiagnosed Neurodevelopmental DisordersYe Cao, Ho Ming Luk, Yanyan Zhang, et al.
Pathology|July 4, 2014
Inherited metabolic diseases in the Southern Chinese population: spectrum of diseases and estimated incidence from recurrent mutationsJoannie Hui, Nelson L S Tang, C K Li, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|July 7, 2015
Genetic Interactions Between TRPC6 and NPHS1 Variants Affect Posttransplant Risk of Recurrent Focal Segmental GlomerulosclerosisZ J Sun, K H Ng, P Liao, et al.
HGG Advances|June 18, 2025
Identification of technically challenging variants: Whole-genome sequencing improves diagnostic yield in patients with high clinical suspicion of rare diseasesHau-Yee Ng, Wei Ma, Wai-Kei J Lam, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 11, 2021
Heterozygous loss-of-function variants significantly expand the phenotypes associated with loss of GDF11Thomas A Ravenscroft, Jennifer B Phillips, Elizabeth Fieg, et al.
Epilepsia|May 27, 2021
CSNK2B: A broad spectrum of neurodevelopmental disability and epilepsy severityMichelle E Ernst, Evan H Baugh, Amanda Thomas, et al.
Pageof 2

Showing results (11-20 of 20) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 20 results.
Neonatology|September 9, 2008
Successful treatment of multiple subdural empyemata caused by Mycoplasma hominis in a newbornJosephine S C Chong, Simon Y T Tseung, Hugh S Lam, et al.
Hong Kong Medical Journal = Xianggang Yi Xue Za Zhi|January 26, 2026
Third-trimester prenatal brain imaging for early diagnosis of glutaric aciduria type 1 in monochorionic diamniotic twinsI Y M Wah, Y Cao, N K L Wong, et al.
BMC Medical Ethics|November 2, 2022
The view of Hong Kong parents on secondary use of dried blood spots in newborn screening programL L Hui, E A S Nelson, H B Deng, et al.
Prenatal Diagnosis|December 5, 2009
Noninvasive prenatal exclusion of haemoglobin Bart's using foetal DNA from maternal plasmaSherry S Y Ho, Samuel S C Chong, Evelyn S C Koay, et al.
Frontiers in Genetics|May 2, 2022
Investigation of Chromosomal Structural Abnormalities in Patients With Undiagnosed Neurodevelopmental DisordersYe Cao, Ho Ming Luk, Yanyan Zhang, et al.
Pathology|July 4, 2014
Inherited metabolic diseases in the Southern Chinese population: spectrum of diseases and estimated incidence from recurrent mutationsJoannie Hui, Nelson L S Tang, C K Li, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|July 7, 2015
Genetic Interactions Between TRPC6 and NPHS1 Variants Affect Posttransplant Risk of Recurrent Focal Segmental GlomerulosclerosisZ J Sun, K H Ng, P Liao, et al.
HGG Advances|June 18, 2025
Identification of technically challenging variants: Whole-genome sequencing improves diagnostic yield in patients with high clinical suspicion of rare diseasesHau-Yee Ng, Wei Ma, Wai-Kei J Lam, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 11, 2021
Heterozygous loss-of-function variants significantly expand the phenotypes associated with loss of GDF11Thomas A Ravenscroft, Jennifer B Phillips, Elizabeth Fieg, et al.
Epilepsia|May 27, 2021
CSNK2B: A broad spectrum of neurodevelopmental disability and epilepsy severityMichelle E Ernst, Evan H Baugh, Amanda Thomas, et al.
Pageof 2