Thorough analysis of unorthodox ABO deletions called by the 1000 Genomes project.

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Thorough analysis of unorthodox ABO deletions called by the 1000 Genomes project.

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

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2017年学术文章

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Thorough analysis of unorthodox ABO deletions called by the 1000 Genomes project.

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Thorough analysis of unorthodox ABO deletions called by the 1000 Genomes project.

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Thorough analysis of unorthodox ABO deletions called by the 1000 Genomes project.

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Thorough analysis of unorthodox ABO deletions called by the 1000 Genomes project.

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Thorough analysis of unorthodox ABO deletions called by the 1000 Genomes project.

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Thorough analysis of unorthodox ABO deletions called by the 1000 Genomes project.

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P1476

Thorough analysis of unorthodox ABO deletions called by the 1000 Genomes project

@en

P2093

M L Olsson

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Å Hellberg

http://www.w3.org/2001/XMLSchema#string

P2860

Initial sequencing and analysis of the human genome

The Sequence Ontology: a tool for the unification of genome annotations

An integrated map of genetic variation from 1,092 human genomes

A map of human genome variation from population-scale sequencing

ABO exon and intron analysis in individuals with the AweakB phenotype reveals a novel O1v-A2 hybrid allele that causes four missense mutations in the A transferase

A global reference for human genetic variation

Analysis of protein-coding genetic variation in 60,706 humans

Missense mutation of FUT1 and deletion of FUT2 are responsible for Indian Bombay phenotype of ABO blood group system

Integrative Genomics Viewer (IGV): high-performance genomics data visualization and exploration

Origins and functional impact of copy number variation in the human genome

P304

185-197

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P31

scholarly article

P356

10.1111/VOX.12613

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P433

http://www.w3.org/2001/XMLSchema#string

P478

113

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P50

M Möller

M L Olsson

Åsa Hellberg

P577

2017-12-06T00:00:00Z

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P698

29214632

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