Publications:

Deep phenotyping and whole-exome sequencing improved the diagnostic yield for nuclear pedigrees with neurodevelopmental disorders.

Molecular Genetics & Genomic Medicine

Wang, Qingqing Q; Tang, Xia X; Yang, Ke K; Huo, Xiaodong X; Zhang, Hui H; Ding, Keyue K; Liao, Shixiu S

Publication Date: 2022-05

Variant appearance in text: BRAF: 763C>T

PubMed Link: 35266334

Variant Present in the following documents:

• MGG3-10-e1918.pdf

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Circulating tumour DNA sequence analysis as an alternative to multiple myeloma bone marrow aspirates.

Nature Communications

Kis, Olena O; Kaedbey, Rayan R; Chow, Signy S; Danesh, Arnavaz A; Dowar, Mark M; Li, Tiantian T; Li, Zhihua Z; Liu, Jessica J; Mansour, Mark M; Masih-Khan, Esther E; Zhang, Tong T; Bratman, Scott V SV; Oza, Amit M AM; Kamel-Reid, Suzanne S; Trudel, Suzanne S; Pugh, Trevor J TJ

Publication Date: 2017-05-11

Variant appearance in text: BRAF: 763C>T

PubMed Link: 28492226

Variant Present in the following documents:

• ncomms15086-s3.xlsx, sheet 1

View BVdb publication page