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

Results: 21

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
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
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
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
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
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
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
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