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PubPharm (44)
1
Inherited CD19 Deficiency Does Not Impair Plasma Cell Formation or Response to CXCL12
enthalten in:
Journal of clinical immunology
| 2023
von
Walker, K.
|
Mistry, A.
|
Watson, C.
| +9
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2
Haplotyping Using Long-Range PCR and Nanopore Sequencing to Phase Variants : Lessons Learned From the ABCA4 Locus
enthalten in:
Laboratory investigation; a journal of technical methods and pathology
| 2023
von
McClinton, B.
|
Watson, C.
|
Crinnion, L.
| +4
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3
Long-Read Nanopore Sequencing of RPGR ORF15 is Enhanced Following DNase I Treatment of MinION Flow Cells
enthalten in:
Molecular diagnosis & therapy
| 2023
von
Yahya, S.
|
Watson, C.
|
Carr, I.
| +9
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4
Targeted nanopore sequencing enables complete characterisation of structural deletions initially identified using exon-based short-read sequencing strategies
enthalten in:
Molecular genetics & genomic medicine
| 2023
von
McClinton, B.
|
Crinnion, L.
|
McKibbin, M.
| +7
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5
Long-Read Nanopore Sequencing of RPGR ORF15 is Enhanced Following DNase I Treatment of MinION Flow Cells
enthalten in:
Molecular diagnosis & therapy
| 2023
von
Yahya, S.
|
Watson, C.
|
Carr, I.
| +9
Wird geladen...
6
Long-Read Nanopore Sequencing of RPGR ORF15 is Enhanced Following DNase I Treatment of MinION Flow Cells
enthalten in:
Molecular diagnosis & therapy
| 2023
von
Yahya, S.
|
Watson, C.
|
Carr, I.
| +9
Wird geladen...
7
Long-Read Nanopore Sequencing of RPGR ORF15 is Enhanced Following DNase I Treatment of MinION Flow Cells
enthalten in:
Molecular diagnosis & therapy
| 2023
von
Yahya, S.
|
Watson, C.
|
Carr, I.
| +9
Wird geladen...
8
Inherited CD19 Deficiency Does Not Impair Plasma Cell Formation or Response to CXCL12
enthalten in:
Journal of clinical immunology
| 2023
von
Walker, K.
|
Mistry, A.
|
Watson, C.
| +9
Wird geladen...
9
Inherited CD19 Deficiency Does Not Impair Plasma Cell Formation or Response to CXCL12
enthalten in:
Journal of clinical immunology
| 2023
von
Walker, K.
|
Mistry, A.
|
Watson, C.
| +9
Wird geladen...
10
Targeted nanopore sequencing enables complete characterisation of structural deletions initially identified using exon‐based short‐read sequencing strategies
enthalten in:
Molecular Genetics & Genomic Medicine
| 2023
von
McClinton, B.
|
Crinnion, L.
|
McKibbin, M.
| +7
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44
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Molecular diagnosis & therapy
7
Journal of clinical immunology
4
Human mutation
4
Laboratory investigation; a journal of technica...
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BMC medical genetics
3
Journal of medical genetics
1
American journal of human genetics
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American journal of medical genetics. Part A
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Journal of obstetrics and gynaecology : the jou...
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South African medical journal = Suid-Afrikaanse...
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The Journal of molecular diagnostics : JMD
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Thema
23
Journal Article
12
Research Support, Non-U.S. Gov't
6
Case Reports
3
CD19
3
CXCR4
3
antibody deficiency
3
plasma cells
3
software
2
CNV
2
Dyneins
2
EC 2.3.2.27
2
EC 2.7.11.1
2
EC 3.6.1.-
2
EC 3.6.1.3
2
EC 3.6.4.2
2
Exome
2
Eye Proteins
2
Joubert
2
Meckel-Gruber
2
Mismatch Repair Endonuclease PMS2
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Erscheinungszeitraum
18
2020-
26
2010-2019
Erscheinungsjahr(e)
Von:
Bis:
Sprache
40
Englisch
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