(Q57289470)

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Absence of chromosome 19q13.41 amplification in a case of atypical teratoid/rhabdoid tumor with ependymoblastic differentiation

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Absence of chromosome 19q13.41 amplification in a case of atypical teratoid/rhabdoid tumor with ependymoblastic differentiation (English)

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Stefan Pfister

2

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Marco Gessi

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1

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Marco Gessi

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Andrey Korshunov

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4

object named as

Andrey Korshunov

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author name string

Volkmar H. Hans

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3

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Torsten Pietsch

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5

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publication date

18 November 2010

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published in

Acta Neuropathologica

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volume

121

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issue

2

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page(s)

283-285

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exact match

https://scigraph.springernature.com/pub.10.1007/s00401-010-0778-7

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cites work

Atypical teratoid/rhabdoid tumor of the central nervous system: a highly malignant tumor of infancy and childhood frequently mistaken for medulloblastoma: a Pediatric Oncology Group study

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https://api.crossref.org/works/10.1007%2FS00401-010-0778-7

retrieved

21 January 2018

Embryonal tumors with abundant neuropil and true rosettes: a distinctive CNS primitive neuroectodermal tumor

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Crossref

reference URL

https://api.crossref.org/works/10.1007%2FS00401-010-0778-7

retrieved

21 January 2018

Ependymoblastoma: dear, damned, distracting diagnosis, farewell!*.

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Crossref

reference URL

https://api.crossref.org/works/10.1007%2FS00401-010-0778-7

retrieved

21 January 2018

Focal genomic amplification at 19q13.42 comprises a powerful diagnostic marker for embryonal tumors with ependymoblastic rosettes.

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https://api.crossref.org/works/10.1007%2FS00401-010-0778-7

retrieved

21 January 2018

Frequent amplification of a chr19q13.41 microRNA polycistron in aggressive primitive neuroectodermal brain tumors

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Crossref

reference URL

https://api.crossref.org/works/10.1007%2FS00401-010-0778-7

retrieved

21 January 2018

Molecular diagnostics of CNS embryonal tumors

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Crossref

reference URL

https://api.crossref.org/works/10.1007%2FS00401-010-0778-7

retrieved

21 January 2018

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DOI

10.1007/S00401-010-0778-7

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PubMed ID

21086133

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(Q57289470)

Absence of chromosome 19q13.41 amplification in a case of atypical teratoid/rhabdoid tumor with ependymoblastic differentiation

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