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Sequencing individual genomes with recurrent genomic disorder deletions: an approach to characterize genes for autosomal recessive rare disease traits.
Published in:
Genome Medicine, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13073-022-01113-y
By:
- Yuan, Bo;
- Schulze, Katharina V.;
- Assia Batzir, Nurit;
- Sinson, Jefferson;
- Dai, Hongzheng;
- Zhu, Wenmiao;
- Bocanegra, Francia;
- Fong, Chin-To;
- Holder, Jimmy;
- Nguyen, Joanne;
- Schaaf, Christian P.;
- Yang, Yaping;
- Bi, Weimin;
- Eng, Christine;
- Shaw, Chad;
- Lupski, James R.;
- Liu, Pengfei
Publication type:
Article
Response to Hypomethylating Agents in Myelodysplastic Syndrome Is Associated With Emergence of Novel TCR Clonotypes.
Published in:
Frontiers in Immunology, 2021, v. 11, p. N.PAG, doi. 10.3389/fimmu.2021.659625
By:
- Abbas, Hussein A.;
- Reville, Patrick K.;
- Jiang, Xianli;
- Yang, Hui;
- Reuben, Alexandre;
- Im, Jin Seon;
- Little, Latasha;
- Sinson, Jefferson C.;
- Chen, Ken;
- Futreal, Andrew;
- Garcia-Manero, Guillermo
Publication type:
Article