Weiwei Sun

7.

Xuliang Zhao, Weiwei Sun, Jian-an Jia, 1966, The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians.

7.

Xuliang Zhao, Weiwei Sun, Jian-an Jia, 2020, The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians.

Humus Components and Biogenic Structures under Tropical Slash-and- 1 Burn Agriculture 2 3

Xuliang Zhao, Weiwei Sun, Jian-an Jia, 2010 .

Compound Heterozygous Mutations in ABCG5 or ABCG8 Causing Chinese Familial Sitosterolemia.

Weiwei Sun, Yajian Wang, Gong Zhang, 2020, The journal of gene medicine.

Prenatal ultrasound-assisted identification of multiple malformations caused by a deletion in the long-arm end of chromosome 7 and review of the literature

Xuliang Zhao, Weiwei Sun, Jian-an Jia, 2020, The Journal of Maternal-Fetal & Neonatal Medicine.

Prenatal case report of Barth syndrome caused by novel TAFAZZIN mutation: Clinical characteristics of fetal dilated cardiomyopathy with ascites

Xuliang Zhao, Weiwei Sun, Jian-an Jia, 2022, Frontiers in Pediatrics.

Clinical report and genetic analysis of a neonate with genitourinary and/or brain malformation syndrome caused by a non‐coding sequence variant of PPP1R12A

Weiwei Sun, Zhen Zhang, Xin Chen, 2023, Molecular genetics & genomic medicine.

Case report: “Major fetal cardiac pathology associated with a novel CTNND1 mutation”

Xuliang Zhao, Weiwei Sun, Zhuojun Wei, 2023, Frontiers in Pediatrics.

COL7A1 Homozygous Arg2471Ter Mutation Leads to the Severe Phenotype of Autosomal Recessive Dystrophic Epidermolysis Bullosa in the Fetus

Xuliang Zhao, Weiwei Sun, Ruixia Tian, 2022, Molecular Syndromology.

Rare hypomagnesemia, seizures, and mental retardation in a 4‐month‐old patient caused by novel CNNM2 mutation Tyr189Cys: Genetic analysis and review

Weiwei Sun, De Wu, Shu Hou, 2022, Molecular genetics & genomic medicine.

Usher syndrome type 2A complicated with glycogen storage disease type 3 due to paternal uniparental isodisomy of chromosome 1 in a sporadic patient

Weiwei Sun, Yajian Wang, Weiyue Gu, 2021, Molecular genetics & genomic medicine.

Nutrient Control of Hunger by Extrinsic Gastrointestinal

Xuliang Zhao, Weiwei Sun, Jian-an Jia, 2013 .