Publications:

Exome sequencing in fetuses with short long bones detected by ultrasonography: A retrospective cohort study.

Frontiers In Genetics

Huang, Yanlin Y; Liu, Chang C; Ding, Hongke H; Wang, Yunan Y; Yu, Lihua L; Guo, Fangfang F; Li, Fake F; Shi, Xiaomei X; Zhang, Yan Y; Yin, Aihua A

Publication Date: 2023

Variant appearance in text: CD36: 429+3dup

PubMed Link: 36923788

Variant Present in the following documents:

• Table3.xlsx, sheet 1

View BVdb publication page

Whole exome sequencing for diagnosis of hereditary thrombocytopenia.

Medicine

Mekchay, Ponthip P; Ittiwut, Chupong C; Ittiwut, Rungnapa R; Akkawat, Benjaporn B; Le Grand, Supang Maneesri SM; Leela-Adisorn, Netchanok N; Muanpetch, Suwanna S; Khovidhunkit, Weerapan W; Sosothikul, Darintr D; Shotelersuk, Vorasuk V; Suphapeetiporn, Kanya K; Rojnuckarin, Ponlapat P

Publication Date: 2020-11-20

Variant appearance in text: CD36: 429+3dupG

PubMed Link: 33217855

Variant Present in the following documents:

• Main text
• medi-99-e23275.pdf

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The ChinaMAP analytics of deep whole genome sequences in 10,588 individuals.

Cell Research

Cao, Yanan Y; Li, Lin L; Xu, Min M; Feng, Zhimin Z; Sun, Xiaohui X; Lu, Jieli J; Xu, Yu Y; Du, Peina P; Wang, Tiange T; Hu, Ruying R; Ye, Zhen Z; Shi, Lixin L; Tang, Xulei X; Yan, Li L; Gao, Zhengnan Z; Chen, Gang G; Zhang, Yinfei Y; Chen, Lulu L; Ning, Guang G; Bi, Yufang Y; Wang, Weiqing W; ,

Publication Date: 2020-09

Variant appearance in text: CD36: 429+3dupG; rs777551390

PubMed Link: 32355288

Variant Present in the following documents:

• 41422_2020_322_MOESM14_ESM.xlsx, sheet 1

View BVdb publication page