Works matching IS 13899600 AND DT 2006 AND VI 5 AND IP 2

Results: 15

A Novel Exon Duplication Event Leading to a Truncating Germ-line Mutation of the APC Gene in a Familial Adenomatous Polyposis Family.

Published in:

Familial Cancer, 2006, v. 5, n. 2, p. 205, doi. 10.1007/s10689-006-7471-y

By:

Amy McCart;
Andrew Latchford;
Emmanouil Volikos;
Andrew Rowan;
Ian Tomlinson;
Andrew Silver

Publication type:

Article

Interleukin-10 Polymorphisms, Cancer Susceptibility and Prognosis.

Published in:

Familial Cancer, 2006, v. 5, n. 2, p. 143, doi. 10.1007/s10689-005-0072-3

By:

W. Howell;
Matthew Rose-Zerilli

Publication type:

Article

Familial Cancer (special issue) Breast Cancer Treatment and Genetics.

Published in:

Familial Cancer, 2006, v. 5, n. 2, p. 127, doi. 10.1007/s10689-006-7904-7

By:

Diana Eccles

Publication type:

Article

BRCA1 and BRCA2: Chemosensitivity, Treatment Outcomes and Prognosis.

Published in:

Familial Cancer, 2006, v. 5, n. 2, p. 135, doi. 10.1007/s10689-005-2832-5

By:

William Foulkes

Publication type:

Article

Germline Mutations of the hMLH1 and hMSH2 Mismatch Repair Genes in Belgian Hereditary Nonpolyposis Colon Cancer (HNPCC) Patients.

Published in:

Familial Cancer, 2006, v. 5, n. 2, p. 179, doi. 10.1007/s10689-005-5958-6

By:

M. Spaepen;
B. Vankeirsbilck;
S. Van Opstal;
S. Tejpar;
E. Van Cutsem;
K. Geboes;
E. Legius;
G. Matthijs

Publication type:

Article

Desmoid Tumors – a Characterization of Patients Seen at Mayo Clinic 1976–1999.

Published in:

Familial Cancer, 2006, v. 5, n. 2, p. 191, doi. 10.1007/s10689-005-5959-5

By:

Taya Fallen;
Marcia Wilson;
Bruce Morlan;
Noralane Lindor

Publication type:

Article

Determinants of Preferences for Genetic Counselling in Jewish Women.

Published in:

Familial Cancer, 2006, v. 5, n. 2, p. 159, doi. 10.1007/s10689-005-3871-7

By:

Carmel Apicella;
Stuart Peacock;
Lesley Andrews;
Katherine Tucker;
Agnes Bankier;
Mary Daly;
John Hopper

Publication type:

Article

Part II Regular Articles.

Published in:: Familial Cancer, 2006, v. 5, n. 2, p. 158, doi. 10.1007/s10689-006-8162-4
Publication type:: Article

The RET Mutation E768D Confers a Late-onset Familial Medullary Thyroid Carcinoma – Only Phenotype with Incomplete Penetrance: Implications for Screening and Management of Carrier Status.

Published in:

Familial Cancer, 2006, v. 5, n. 2, p. 201, doi. 10.1007/s10689-006-6990-x

By:

Tabib Dabir;
Steven Hunter;
Colin Russell;
Damien McCall;
Patrick Morrison

Publication type:

Article

Late-Onset Common Cancers in a Kindred with an Arg213Gln TP53 Germline Mutation.

Published in:

Familial Cancer, 2006, v. 5, n. 2, p. 169, doi. 10.1007/s10689-005-4789-9

By:

Mariëlle Ruijs;
Senno Verhoef;
Gea Wigbout;
Roelof Pruntel;
Arno Floore;
Daphne de Jong;
Laura van ′t Veer;
Fred Menko

Publication type:

Article

Pharmacogenetics in the Management of Breast Cancer – Prospects for Individualised Treatment.

Published in:

Familial Cancer, 2006, v. 5, n. 2, p. 151, doi. 10.1007/s10689-005-3241-5

By:

Fiona Blackhall;
Sacha Howell;
Bill Newman

Publication type:

Article

Part I Special Issue: Breast Cancer Treatment and Genetics.

Published in:: Familial Cancer, 2006, v. 5, n. 2, p. 1, doi. 10.1007/s10689-006-8161-5
Publication type:: Article

A ‘Nonsense’ Mutation Leads to Aberrant Splicing of hMLH1 in a German Hereditary Non-polyposis Colorectal Cancer Family.

Published in:

Familial Cancer, 2006, v. 5, n. 2, p. 195, doi. 10.1007/s10689-006-6988-4

By:

J. Baehring;
C. Sutter;
M. Kadmon;
M. Doeberitz;
J. Gebert

Publication type:

Article

Compliance and Satisfaction with Long-Term Surveillance in Finnish HNPCC Families.

Published in:

Familial Cancer, 2006, v. 5, n. 2, p. 175

By:

Kirsi Pylvänäinen;
Matti Kairaluoma;
Jukka-Pekka Mecklin

Publication type:

Article

Genotype Phenotype Correlation in Li-Fraumeni Syndrome Kindreds and its Implications for Management.

Published in:

Familial Cancer, 2006, v. 5, n. 2, p. 129, doi. 10.1007/s10689-005-4522-8

By:

R. Moule;
S. Jhavar;
R. Eeles

Publication type:

Article