Publications by authors named "Dilys M Parry"

11Publications

Clinical features distinguish childhood chordoma associated with tuberous sclerosis complex (TSC) from chordoma in the general paediatric population.

J Med Genet 2011 Jul 25;48(7):444-9. Epub 2011 Jan 25.

Genetic Epidemiology Branch, Human Genetics Program, Division of Cancer Epidemiologyand Genetics, National Cancer Institute, National Institutes of Health, Department of Health and Human Services, Bethesda, Maryland, USA.

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July 2011

Monozygotic twins discordant for neurofibromatosis 1.

Am J Med Genet A 2010 Mar;152A(3):601-6

Center for Human Genetic Research, Massachusetts General Hospital, Boston, Massachusetts 02114, USA.

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March 2010

T (brachyury) gene duplication confers major susceptibility to familial chordoma.

Nat Genet 2009 Nov 4;41(11):1176-8. Epub 2009 Oct 4.

Division of Cancer Epidemiology & Genetics, National Cancer Institute, National Institutes of Health, Department of Health and Human Services, Bethesda, MD, USA.

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November 2009

Neurofibromatosis type 2.

Lancet 2009 Jun 22;373(9679):1974-86. Epub 2009 May 22.

Surgical Neurology Branch, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD 20892-1414, USA.

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June 2009

NF2 and spinal tumors.

Authors:
Dilys M Parry

J Neurosurg Spine 2006 Aug;5(2):179; author reply 179

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August 2006

Predictors of vestibular schwannoma growth in patients with neurofibromatosis Type 2.

J Neurosurg 2002 Feb;96(2):217-22

Department of Radiology, Georgetown University Medical Center, Washington, DC, USA.

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February 2002