Diagnosis of distal 22q11.2 deletion syndrome in a patient with a teratoid/rhabdoid tumour
about
Constitutional chromosomal events at 22q11 and 15q26 in a child with a pilocytic astrocytoma of the spinal cord.Significant evidence of linkage for a gene predisposing to colorectal cancer and multiple primary cancers on 22q11.Molecular Transition of an Adult Low-Grade Brain Tumor to an Atypical Teratoid/Rhabdoid Tumor Over a Time-Course of 14 Years.The recurrent distal 22q11.2 microdeletions are often de novo and do not represent a single clinical entity: a proposed categorization system.Adult-onset atypical teratoid/rhabdoid tumor featuring long spindle cells with nuclear palisading and perivascular pseudorosettes.The immune deficiency of chromosome 22q11.2 deletion syndrome.
P2860
Diagnosis of distal 22q11.2 deletion syndrome in a patient with a teratoid/rhabdoid tumour
description
scientific article published on 25 December 2010
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wetenschappelijk artikel
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наукова стаття, опублікована в травні 2011
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name
Diagnosis of distal 22q11.2 de ...... ith a teratoid/rhabdoid tumour
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Diagnosis of distal 22q11.2 de ...... ith a teratoid/rhabdoid tumour
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type
label
Diagnosis of distal 22q11.2 de ...... ith a teratoid/rhabdoid tumour
@en
Diagnosis of distal 22q11.2 de ...... ith a teratoid/rhabdoid tumour
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prefLabel
Diagnosis of distal 22q11.2 de ...... ith a teratoid/rhabdoid tumour
@en
Diagnosis of distal 22q11.2 de ...... ith a teratoid/rhabdoid tumour
@nl
P2093
P1476
Diagnosis of distal 22q11.2 de ...... ith a teratoid/rhabdoid tumour
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P2093
P304
P356
10.1016/J.EJMG.2010.12.007
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2010-12-25T00:00:00Z