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Sequencing individual genomes with recurrent genomic disord..:

Yuan, Bo ; Schulze, Katharina V ; Assia Batzir, Nurit...
Yuan, Bo, Schulze, Katharina V., Assia Batzir, Nurit, et al. "Sequencing individual genomes with recurrent genomic disorder deletions: an approach to characterize genes for autosomal recessive rare disease traits." Genome Medicine, 14, (2022) Springer Nature: https://doi.org/10.1186/s13073-022-01113-y.. , 2022

Link: https://hdl.handle.net/1911/113773

RT Journal
T1 <Title>Sequencing individual genomes with recurrent genomic disorder deletions: an approach to characterize genes for autosomal recessive rare disease traits</Title>

UL https://suche.suub.uni-bremen.de/peid=base-ftriceuniv:oai:scholarship.rice.edu:1911_113773&Exemplar=1&LAN=DE
				
A1 Yuan, Bo
A1 Schulze, Katharina V
A1 Assia Batzir, Nurit
A1 Sinson, Jefferson
A1 Dai, Hongzheng
A1 Zhu, Wenmiao
A1 Bocanegra, Francia
A1 Fong, Chin-To
A1 Holder, Jimmy
A1 Nguyen, Joanne
A1 Schaaf, Christian P
A1 Yang, Yaping
A1 Bi, Weimin
A1 Eng, Christine
A1 Shaw, Chad
A1 Lupski, James R
A1 Liu, Pengfei
PB Springer Nature
YR 2022
JF Yuan, Bo, Schulze, Katharina V., Assia Batzir, Nurit, et al. "Sequencing individual genomes with recurrent genomic disorder deletions: an approach to characterize genes for autosomal recessive rare disease traits." Genome Medicine, 14, (2022) Springer Nature: https://doi.org/10.1186/s13073-022-01113-y.
LK http://dx.doi.org/https://hdl.handle.net/1911/113773
DO https://hdl.handle.net/1911/113773
SF ELIB - SuUB Bremen

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