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Shengkai Wei
Observed name:
Wei, Shengkai
Institution:
Guangxi Maternal and Child Health Hospital
Observed institution:
Guangxi Maternal and Child Health Hospital
OpenAlex ID:
A5113890161
Prenatal diagnosis of cri-du-chat syndrome by SNP array: report of twelve cases and review of the literature
2019
·
Jiasun Su
, Huayu Fu
, et al.
·
Molecular Cytogenetics
·
13
PDF
Assessing the clinical application value of SNP-array in fetal central nervous system malformations
2025
·
Wei Li
, Jiasun Su
, et al.
·
Human Genomics
·
3
PDF
TARS2 c.470 C > G is a chinese-specific founder mutation in three unrelated families with mitochondrial encephalomyopathy
2024
·
Shujie Zhang
, Haisong Qin
, et al.
·
Orphanet Journal of Rare Diseases
·
1
PDF
Clinical and genetic profiles of postnatal patients with skeletal dysplasia in Guangxi during 8 years: a single-center experience
2026
·
Sheng Yi
, Qi Yang
, et al.
·
Orphanet Journal of Rare Diseases
PDF
Additional file 2 of Clinical and genetic profiles of postnatal patients with skeletal dysplasia in Guangxi during 8 years: a single-center experience
2026
·
Sheng Yi
, Qi Yang
, et al.
·
Figshare
Additional file 5 of Clinical and genetic profiles of postnatal patients with skeletal dysplasia in Guangxi during 8 years: a single-center experience
2026
·
Sheng Yi
, Qi Yang
, et al.
·
Figshare
Additional file 7 of Clinical and genetic profiles of postnatal patients with skeletal dysplasia in Guangxi during 8 years: a single-center experience
2026
·
Sheng Yi
, Qi Yang
, et al.
·
Figshare
Additional file 6 of Clinical and genetic profiles of postnatal patients with skeletal dysplasia in Guangxi during 8 years: a single-center experience
2026
·
Sheng Yi
, Qi Yang
, et al.
·
Figshare
Additional file 8 of Clinical and genetic profiles of postnatal patients with skeletal dysplasia in Guangxi during 8 years: a single-center experience
2026
·
Sheng Yi
, Qi Yang
, et al.
·
Figshare
Additional file 4 of Clinical and genetic profiles of postnatal patients with skeletal dysplasia in Guangxi during 8 years: a single-center experience
2026
·
Sheng Yi
, Qi Yang
, et al.
·
Figshare
Additional file 1 of Clinical and genetic profiles of postnatal patients with skeletal dysplasia in Guangxi during 8 years: a single-center experience
2026
·
Sheng Yi
, Qi Yang
, et al.
·
Figshare
Additional file 3 of Clinical and genetic profiles of postnatal patients with skeletal dysplasia in Guangxi during 8 years: a single-center experience
2026
·
Sheng Yi
, Qi Yang
, et al.
·
Figshare
Clinical and Genetic Analysis of SMARCC2 ‐Related Diseases in Three Chinese Patients
2026
·
Shan Ou
, Shujie Zhang
, et al.
·
Molecular Genetics & Genomic Medicine
16p13.11 deletion/duplication: a large cohort study on prenatal diagnosis, postnatal outcomes, and phenotypic manifestations
2025
·
Xianglian Tang
, Jiasun Su
, et al.
·
BMC Pregnancy and Childbirth
PDF
A novel dinucleotide variant at 5′ splice sites in the F8 gene causes exon 19 skipping in a Chinese family with hemophilia A
2025
·
Xunzhao Zhou
, Qi Yang
, et al.
·
Frontiers in Genetics
PDF
16p13.11 deletion/duplication: a large cohort study on prenatal diagnosis, postnatal outcomes, and phenotypic manifestations
2025
·
Tang, Xianglian
, Su, Jiasun
, et al.
·
Figshare
Additional file 1 of 16p13.11 deletion/duplication: a large cohort study on prenatal diagnosis, postnatal outcomes, and phenotypic manifestations
2025
·
Tang, Xianglian
, Su, Jiasun
, et al.
·
Figshare
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Works count:
21
Citation count:
17
H-index:
2
I10-index:
1
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