1 Pilot study of a novel multi-functional noninvasive prenatal test on fetus aneuploidy, copy number v..
来源:MOL GENET GENOM MED( P 2324-9269 E ) 发表时间: 2019/04
类型:期刊论文 为本人加分:748.223831
2 Non-invasive prenatal screening for Emanuel syndrome
来源:MOL CYTOGENET( P E 1755-8166 ) 发表时间: 2020/03
类型:期刊论文 为本人加分:261.249235
贡献度:单独第一作者
3 Different segregation patterns in five carriers due to a pericentric inversion of chromosome 1
来源:SYST BIOL REPROD MED( P 1939-6368 E 1939-6376 ) 发表时间: 2014/12
类型:期刊论文 为本人加分:205.650953
贡献度:单独第一作者
4 Heterozygous Deletion of the SHOX Gene Enhancer in two Females With Clinical Heterogeneity Associati..
来源:FRONT GENET( P E 1664-8021 ) 发表时间: 2019/11
类型:期刊论文 为本人加分:178.362267
贡献度:参与作者
5 Serum and Glucocorticoid Regulated Kinase 1 in Sodium Homeostasis
来源:INT J MOL SCI( P E 1422-0067 ) 发表时间: 2016/08
类型:期刊论文 为本人加分:103.602792
贡献度:参与作者
6 Lack of MECP2 gene transcription on the duplicated alleles of two related asymptomatic females with ..
来源:HUM MUTAT( P 1059-7794 E 1098-1004 ) 发表时间: 2021/11
类型:期刊论文 为本人加分:73.558114
贡献度:参与作者
7 Preimplantation genetic diagnosis and screening (PGD/S) using a semiconductor sequencing platform
来源:HUM GENOMICS( P 1473-9542 E 1479-7364 ) 发表时间: 2019/01
类型:期刊论文 为本人加分:70.147289
贡献度:参与作者
8 Fetal mosaic trisomy 2q associated with polydactyly
来源:INT J CLIN EXP MED( P 1940-5901 E ) 发表时间: 2018/01
类型:期刊论文 为本人加分:48.657264
9 Detection of fetal duplication 16p11.2q12.1 by next-generation sequencing of maternal plasma and inv..
来源:J MATERN-FETAL NEO M( P 1476-7058 E 1476-4954 ) 发表时间: 2019/01
类型:期刊论文 为本人加分:21.290428
贡献度:参与作者
10 A copy number variation genotyping method for aneuploidy detection in spontaneous abortion specimens
来源:PRENATAL DIAG( P 0197-3851 E 1097-0223 ) 发表时间: 2017/02
类型:期刊论文 为本人加分:5.272993
贡献度:参与作者