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Isolation of a gene encoding an integral membrane protein from the vicinity of a balanced translocation breakpoint associated with DiGeorge syndrome
by
Wadey, Roy
,
Daw, Sara
,
Taylor, Catherine
,
Atif, Uzma
,
Kamath, Shalan
,
Halford, Stephanie
,
O‘Donnell, Hilary
,
Wilson, David
,
Goodship, Judith
,
Burn, John
,
Scambler, Peter
Published in
Human molecular genetics
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Isolation of a gene expressed during early embryogenesis from the region of 22q11 commonly deleted in DiGeorge syndrome
by
Halford, Stephanie
,
Wilson, David I
,
DAW, Sara C.M.
,
Roberts, Cathrine
,
Wadey, Roy
,
Kamath, Shalan
,
Wickremasinghe, Amal
,
Burn, John
,
Goodship, Judith
,
Mattel, Marie-Genevieve
,
Moormon, F.M.
,
Sclambler, Peter J.
Published in
Human molecular genetics
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Human Molecular Genetics
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Hum Mol Genet
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Amino Acid Sequence
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Biochemistry & Molecular Biology
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Biological And Medical Sciences
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Chromosome Mapping
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Chromosomes, Human, Pair 22
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Digeorge Syndrome - Genetics
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Genetics & Heredity
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Humans
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Immunodeficiencies
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Immunodeficiencies. Immunoglobulinopathies
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Immunopathology
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Life Sciences & Biomedicine
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Medical Sciences
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Molecular Sequence Data
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Science & Technology
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Animals
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Bacteriophage P1
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Base Sequence
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Chromosome 22
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Deletion
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Oxford Journals Online
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