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PubPharm (18)
1
Haplotype analysis in Preimplantation Genetic Testing for Special Monogenic Diseases Cases based on Nanopore Sequencing
enthalten in:
ResearchSquare.com
| 2024
von
He, S.
|
Zhang, Z.
|
Xu, L.
| +8
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2
Comprehensive analysis of genomic complexity in the 5’ end coding region of the DMD gene in patients of exons 1-2 duplications based on long-read sequencing
enthalten in:
ResearchSquare.com
| 2024
von
Shen, J.
|
Ding, T.
|
Sun, X.
| +8
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3
Comprehensive analysis of genomic complexity in the 5' end coding region of the DMD gene in patients of exons 1-2 duplications based on long-read sequencing
enthalten in:
BMC genomics
| 2024
von
Shen, J.
|
Ding, T.
|
Sun, X.
| +8
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4
Comprehensive analysis of genomic complexity in the 5’ end coding region of the DMD gene in patients of exons 1–2 duplications based on long-read sequencing
enthalten in:
BMC genomics
| 2024
von
Shen, J.
|
Ding, T.
|
Sun, X.
| +8
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5
Nanopore sequencing with T2T-CHM13 for accurate detection and preventing the transmission of structural rearrangements in highly repetitive heterochromatin regions in human embryos
enthalten in:
Clinical and translational medicine
| 2024
von
Xia, Q.
|
Ding, T.
|
Chang, T.
| +11
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6
Nanopore sequencing with T2T‐CHM13 for accurate detection and preventing the transmission of structural rearrangements in highly repetitive heterochromatin regions in human embryos
enthalten in:
Clinical and Translational Medicine
| 2024
von
Xia, Q.
|
Ding, T.
|
Chang, T.
| +11
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7
Clinical application of nanopore sequencing for haplotype linkage analysis in preimplantation genetic testing for Duchenne muscular dystrophy
enthalten in:
ResearchSquare.com
| 2023
von
Xia, Q.
|
Chang, T.
|
Ding, T.
| +4
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8
A long-read sequencing and SNP haplotype-based novel preimplantation genetic testing method for female ADPKD patient with de novo PKD1 mutation
enthalten in:
ResearchSquare.com
| 2023
von
Peng, C.
|
Chen, H.
|
Ren, J.
| +8
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9
A long-read sequencing and SNP haplotype-based novel preimplantation genetic testing method for female ADPKD patient with de novo PKD1 mutation
enthalten in:
BMC genomics
| 2023
von
Peng, C.
|
Chen, H.
|
Ren, J.
| +8
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10
A long-read sequencing and SNP haplotype-based novel preimplantation genetic testing method for female ADPKD patient with de novo PKD1 mutation
enthalten in:
BMC genomics
| 2023
von
Peng, C.
|
Chen, H.
|
Ren, J.
| +8
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18
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Zeitschriftentitel
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BMC genomics
4
ResearchSquare.com
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Thema
8
Journal Article
4
570
4
Biology
3
9007-49-2
3
ADPKD
3
DNA
3
De novo mutation
3
Long read sequencing
3
PGT-M
3
SNP haplotype
2
Aptamers, Nucleotide
2
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2
Dp427c/Dp427m
2
Exonic duplications
2
Long-read sequencing (LRS)
2
MaReCs
2
Nanopore sequencing
2
PGT-SR
2
Preimplantation genetic testing
2
Reciprocal translocation
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Erscheinungszeitraum
15
2020-
3
2010-2019
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