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Whole-exome re-sequencing in a family quartet identifies POP1 mutations as the cause of a novel skeletal dysplasia
by
Glazov, Evgeny A
,
Zankl, Andreas
,
Donskoi, Marina
,
Kenna, Tony J
,
Thomas, Gethin P
,
Clark, Graeme R
,
Duncan, Emma L
,
Brown, Matthew A
Published in
PLoS genetics
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Brief Report: High‐Throughput Sequencing of IL23R Reveals a Low‐Frequency, Nonsynonymous Single‐Nucleotide Polymorphism That Is Associated With Ankylosing Spondylitis in a Han Chin...
by
Davidson, Stuart I.
,
Jiang, Lei
,
Cortes, Adrian
,
Wu, Xin
,
Glazov, Evgeny A.
,
Zheng, Yi
,
Danoy, Patrick A.
,
Liu, Yi
,
Thomas, Gethin P.
,
Brown, Matthew A.
,
Xu, Huji
Published in
Arthritis and rheumatism
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Whole-Exome Re-Sequencing in a Family Quartet Identifies POP1 Mutations As the Cause of a Novel Skeletal Dysplasia: e1002027
by
Glazov, Evgeny A
,
Zankl, Andreas
,
Donskoi, Marina
,
Kenna, Tony J
,
Thomas, Gethin P
,
Clark, Graeme R
,
Duncan, Emma L
,
Brown, Matthew A
Published in
PLoS genetics
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Genome-Wide Analysis of Genetic Alterations In Acute Myeloid Leukaemia (Massively parallel, high-throughput, paired-end DNA sequencing and genotyping of an AML genome)
by
Gray, James X
,
Leo, Paul J
,
Mukhopadhyay, Pamela
,
Glazov, Evgeny A
,
Danoy, Patrick
,
Donskoi, Marina
,
Brown, Anna
,
Lewis, Ian D.
,
D'Andrea, Richard J
,
Brown, Matthew A
,
Marlton, Paula
,
Gill, Devinder S
,
Gonda, Thomas
Published in
Blood
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