(Q42502272)

1 November 2017

title

Rhabdomyosarcoma, Wilms tumor, and deletion of the patched gene in Gorlin syndrome (English)

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1 November 2017

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Mariana M Cajaiba

1

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1 November 2017

Allen E Bale

2

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1 November 2017

Mayra Alvarez-Franco

3

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1 November 2017

Joseph McNamara

4

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1 November 2017

Miguel Reyes-Múgica

5

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1 November 2017

publication date

1 October 2006

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Nature Clinical Practice Oncology

1 November 2017

published in

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1 November 2017

volume

3

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1 November 2017

issue

10

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1 November 2017

page(s)

575-580

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Insulin-like growth factor II is involved in the proliferation control of medulloblastoma and its cerebellar precursor cells

1 November 2017

cites work

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https://api.crossref.org/works/10.1038%2FNCPONC0608

The Third Intergroup Rhabdomyosarcoma Study

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https://api.crossref.org/works/10.1038%2FNCPONC0608

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Mutations of the human homolog of Drosophila patched in the nevoid basal cell carcinoma syndrome

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https://api.crossref.org/works/10.1038%2FNCPONC0608

7 January 2021

Clinical manifestations in 105 persons with nevoid basal cell carcinoma syndrome

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https://api.crossref.org/works/10.1038%2FNCPONC0608

7 January 2021

Nevoid basal cell carcinoma (Gorlin) syndrome

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https://api.crossref.org/works/10.1038%2FNCPONC0608

7 January 2021

Analysis of the PTCH coding region in human rhabdomyosarcoma

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https://api.crossref.org/works/10.1038%2FNCPONC0608

7 January 2021

Deregulation of the hedgehog signalling pathway: a possible role for the PTCH and SUFU genes in human rhabdomyoma and rhabdomyosarcoma development

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https://api.crossref.org/works/10.1038%2FNCPONC0608

7 January 2021

Simultaneous occurrence of Wilms tumor and rhabdomyosarcoma in two patients

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https://api.crossref.org/works/10.1038%2FNCPONC0608

7 January 2021

Cystic Partially Differentiated Nephroblastoma, Embryonal Rhabdomyosarcoma, and Multiple Congenital Anomalies Associated With Variegated Mosaic Aneuploidy and Premature Centromere Division

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https://api.crossref.org/works/10.1038%2FNCPONC0608

7 January 2021

Molecular subtypes and phenotypic expression of Beckwith–Wiedemann syndrome

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https://api.crossref.org/works/10.1038%2FNCPONC0608

7 January 2021

Disruption of imprinted genes at chromosome region 11p15.5 in paediatric rhabdomyosarcoma

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https://api.crossref.org/works/10.1038%2FNCPONC0608

7 January 2021

Rhabdomyosarcomas and radiation hypersensitivity in a mouse model of Gorlin syndrome

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https://api.crossref.org/works/10.1038%2FNCPONC0608

7 January 2021

Patched target Igf2 is indispensable for the formation of medulloblastoma and rhabdomyosarcoma.

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https://api.crossref.org/works/10.1038%2FNCPONC0608

7 January 2021

Regulation of rate of cartilage differentiation by Indian hedgehog and PTH-related protein

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https://api.crossref.org/works/10.1038%2FNCPONC0608

7 January 2021

Are myogenin and myoD1 expression specific for rhabdomyosarcoma? A study of 150 cases, with emphasis on spindle cell mimics

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https://api.crossref.org/works/10.1038%2FNCPONC0608

7 January 2021

Effect of duration of treatment on treatment outcome and cost of treatment for Wilms' tumor: a report from the National Wilms' Tumor Study Group

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https://api.crossref.org/works/10.1038%2FNCPONC0608

7 January 2021

Complications of the nevoid basal cell carcinoma syndrome: a case report

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https://api.crossref.org/works/10.1038%2FNCPONC0608

7 January 2021

Genetic predisposition to cancer: the consequences of a delayed diagnosis of Gorlin syndrome

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https://api.crossref.org/works/10.1038%2FNCPONC0608

7 January 2021

Identifiers

DOI

10.1038/NCPONC0608

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1 November 2017

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