Works matching IS 13899600 AND DT 2019 AND VI 18 AND IP 1

Results: 21

Candidate susceptibility variants in angioimmunoblastic T-cell lymphoma.

Published in:

Familial Cancer, 2019, v. 18, n. 1, p. 113, doi. 10.1007/s10689-018-0099-x

By:

Donner, Iikki;
Katainen, Riku;
Kaasinen, Eevi;
Aavikko, Mervi;
Sipilä, Lauri J.;
Pukkala, Eero;
Aaltonen, Lauri A.

Publication type:

Article

International society for gastrointestinal hereditary tumours—InSiGHT.

Published in:: Familial Cancer, 2019, v. 18, n. 1, p. 1, doi. 10.1007/s10689-019-00124-w
Publication type:: Article

The BRCA1 exon 13 duplication: clinical characteristics of 22 families in Northern Sweden.

Published in:

Familial Cancer, 2019, v. 18, n. 1, p. 37, doi. 10.1007/s10689-018-0098-y

By:

Edwinsdotter Ardnor, Christina;
Rosén, Anna;
Ljuslinder, Ingrid;
Melin, Beatrice

Publication type:

Article

Outcome of thyroid ultrasound screening in FAP patients with a normal baseline exam.

Published in:

Familial Cancer, 2019, v. 18, n. 1, p. 75, doi. 10.1007/s10689-018-0097-z

By:

Monachese, Marc;
Mankaney, Gautam;
Lopez, Rocio;
O'Malley, Margaret;
Laguardia, Lisa;
Kalady, Matthew F.;
Church, James;
Shin, Joyce;
Burke, Carol A.

Publication type:

Article

Modified capture-recapture estimates of the number of families with Lynch syndrome in Central Ohio.

Published in:

Familial Cancer, 2019, v. 18, n. 1, p. 67, doi. 10.1007/s10689-018-0096-0

By:

Ranola, John Michael O.;
Pearlman, Rachel;
Hampel, Heather;
Shirts, Brian H.

Publication type:

Article

Capillary electrophoresis as alternative method to detect tumor genetic mutations: the model built on the founder BRCA1 c.4964_4982del19 variant.

Published in:

Familial Cancer, 2019, v. 18, n. 1, p. 29, doi. 10.1007/s10689-018-0094-2

By:

De Bonis, Maria;
Minucci, Angelo;
Scaglione, Giovanni Luca;
De Paolis, Elisa;
Zannoni, Gianfranco;
Scambia, Giovanni;
Capoluongo, Ettore

Publication type:

Article

The development of an online decision aid to support persons having a genetic predisposition to cancer and their partners during reproductive decision-making: a usability and pilot study.

Published in:

Familial Cancer, 2019, v. 18, n. 1, p. 137, doi. 10.1007/s10689-018-0092-4

By:

Reumkens, Kelly;
Tummers, Marly H. E.;
Gietel-Habets, Joyce J. G.;
van Kuijk, Sander M. J.;
Aalfs, Cora M.;
van Asperen, Christi J.;
Ausems, Margreet G. E. M.;
Collée, Margriet;
Dommering, Charlotte J.;
Kets, C. Marleen;
van der Kolk, Lizet E.;
Oosterwijk, Jan C.;
Tjan-Heijnen, Vivianne C. G.;
van der Weijden, Trudy;
de Die-Smulders, Christine E. M.;
van Osch, Liesbeth A. D. M.

Publication type:

Article

Low-level parental mosaicism in an apparent de novo case of Peutz-Jeghers syndrome.

Published in:

Familial Cancer, 2019, v. 18, n. 1, p. 109, doi. 10.1007/s10689-018-0093-3

By:

Butel-Simoes, G. I.;
Spigelman, A. D.;
Scott, R. J.;
Vilain, R. E.

Publication type:

Article

Cholesterol profile in women with premature menopause after risk reducing salpingo-oophorectomy.

Published in:

Familial Cancer, 2019, v. 18, n. 1, p. 19, doi. 10.1007/s10689-018-0091-5

By:

Teixeira, Natalia;
Mourits, Marian J.;
Oosterwijk, Jan C.;
Fakkert, Ingrid E.;
Absalom, Anthony R.;
Bakker, Stephan J. L.;
van der Meer, Peter;
de Bock, Geertruida H.

Publication type:

Article

Identification of a novel GREM1 duplication in a patient with multiple colon polyps.

Published in:

Familial Cancer, 2019, v. 18, n. 1, p. 63, doi. 10.1007/s10689-018-0090-6

By:

McKenna, Danielle B.;
Van Den Akker, Jeroen;
Zhou, Alicia Y.;
Ryan, Lauren;
Leon, Annette;
O'Connor, Robert;
Shah, Payal D.;
Rustgi, Anil K.;
Katona, Bryson W.

Publication type:

Article

The uptake of presymptomatic genetic testing in hereditary breast-ovarian cancer and Lynch syndrome: a systematic review of the literature and implications for clinical practice.

Published in:

Familial Cancer, 2019, v. 18, n. 1, p. 127, doi. 10.1007/s10689-018-0089-z

By:

Menko, Fred H;
ter Stege, Jacqueline A;
van der Kolk, Lizet E;
Jeanson, Kiki N;
Schats, Winnie;
Moha, Daoud Ait;
Bleiker, Eveline M A

Publication type:

Article

Delineating a new feature of constitutional mismatch repair deficiency (CMMRD) syndrome: breast cancer.

Published in:

Familial Cancer, 2019, v. 18, n. 1, p. 105, doi. 10.1007/s10689-018-0088-0

By:

Bush, Lisa;
Aronson, Melyssa;
Tabori, Uri;
Campbell, Brittany B.;
Bedgood, Raymond B.;
Jasperson, Kory

Publication type:

Article

Report of a bi-allelic truncating germline mutation in TP53.

Published in:

Familial Cancer, 2019, v. 18, n. 1, p. 101, doi. 10.1007/s10689-018-0087-1

By:

Brown, Natasha J.;
Bhatia, Kanika;
Teague, Julie;
White, Susan M.;
Lo, Patrick;
Challis, Jackie;
Beshay, Victoria;
Sullivan, Michael;
Malkin, David;
Hansford, Jordan R.

Publication type:

Article

Physician interpretation of variants of uncertain significance.

Published in:

Familial Cancer, 2019, v. 18, n. 1, p. 121, doi. 10.1007/s10689-018-0086-2

By:

Macklin, Sarah K.;
Jackson, Jessica L.;
Atwal, Paldeep S.;
Hines, Stephanie L.

Publication type:

Article

Prevalence of thyroid diseases in familial adenomatous polyposis: a systematic review and meta-analysis.

Published in:

Familial Cancer, 2019, v. 18, n. 1, p. 53, doi. 10.1007/s10689-018-0085-3

By:

Chenbhanich, Jirat;
Atsawarungruangkit, Amporn;
Korpaisarn, Sira;
Phupitakphol, Tanit;
Osataphan, Soravis;
Phowthongkum, Prasit

Publication type:

Article

Sarcoma in neurofibromatosis 2: case report and review of the literature.

Published in:

Familial Cancer, 2019, v. 18, n. 1, p. 97, doi. 10.1007/s10689-018-0084-4

By:

Linder, C.;
Smith, M. J.;
Bulman, M.;
Wallace, A.;
Freemont, A. J.;
Mangham, D. C.;
Evans, D. G. R.

Publication type:

Article

Unsolicited information letters to increase awareness of Lynch syndrome and familial colorectal cancer: reactions and attitudes.

Published in:

Familial Cancer, 2019, v. 18, n. 1, p. 43, doi. 10.1007/s10689-018-0083-5

By:

Petersen, Helle Vendel;
Frederiksen, Birgitte Lidegaard;
Lautrup, Charlotte Kvist;
Lindberg, Lars Joachim;
Ladelund, Steen;
Nilbert, Mef

Publication type:

Article

Reminders of cancer risk and pain catastrophizing: relationships with cancer worry and perceived risk in women with a first-degree relative with breast cancer.

Published in:

Familial Cancer, 2019, v. 18, n. 1, p. 9, doi. 10.1007/s10689-018-0082-6

By:

Whitney, Colette A.;
Dorfman, Caroline S.;
Shelby, Rebecca A.;
Keefe, Francis J.;
Gandhi, Vicky;
Somers, Tamara J.

Publication type:

Article

Hemangioblastoma in Hereditary Leiomyomatosis and Renal Cell Cancer Syndrome: a phenotypic overlap between VHL and HLRCC Syndromes.

Published in:

Familial Cancer, 2019, v. 18, n. 1, p. 91, doi. 10.1007/s10689-018-0081-7

By:

Dow, Eryn;
Winship, Ingrid M.

Publication type:

Article

Germline CDH1 mutations are a significant contributor to the high frequency of early-onset diffuse gastric cancer cases in New Zealand Māori.

Published in:

Familial Cancer, 2019, v. 18, n. 1, p. 83, doi. 10.1007/s10689-018-0080-8

By:

Hakkaart, Christopher;
Ellison-Loschmann, Lis;
Day, Robert;
Sporle, Andrew;
Koea, Jonathan;
Harawira, Pauline;
Cheng, Soo;
Gray, Michelle;
Whaanga, Tracey;
Pearce, Neil;
Guilford, Parry

Publication type:

Article

Clinical and pathologic characteristics of breast cancer patients carrying the c.3481_3491del11 mutation.

Published in:

Familial Cancer, 2019, v. 18, n. 1, p. 1, doi. 10.1007/s10689-018-0079-1

By:

El Tannouri, R.;
Albuisson, E.;
Jonveaux, P.;
Luporsi, E.

Publication type:

Article