Publications:

Noninvasive fetal genotyping of single nucleotide variants and linkage analysis for prenatal diagnosis of monogenic disorders.

Human Genomics

Wu, Wenman W; Zhou, Xuanyou X; Jiang, Zhengwen Z; Zhang, Dazhi D; Yu, Feng F; Zhang, Lanlan L; Wang, Xuefeng X; Chen, Songchang S; Xu, Chenming C

Publication Date: 2022-07-27

Variant appearance in text: rs216901

PubMed Link: 35897115

Variant Present in the following documents:

• 40246_2022_400_MOESM1_ESM.xlsx, sheet 1
• 40246_2022_400_MOESM5_ESM.xlsx, sheet 1
• 40246_2022_Article_400.pdf

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Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study.

Bmc Medical Genetics

Yang, Qiong Q; Kathiresan, Sekar S; Lin, Jing-Ping JP; Tofler, Geoffrey H GH; O'Donnell, Christopher J CJ

Publication Date: 2007-09-19

Variant appearance in text: rs216901

PubMed Link: 17903294

Variant Present in the following documents:

• Main text
• 1471-2350-8-S1-S12.pdf

View BVdb publication page