Works matching IS 13899600 AND DT 2017 AND VI 16 AND IP 3

Results: 20

Detection of false positive mutations in BRCA gene by next generation sequencing.

Published in:

Familial Cancer, 2017, v. 16, n. 3, p. 311, doi. 10.1007/s10689-016-9955-8

By:

Suryavanshi, Moushumi;
Kumar, Dushyant;
Panigrahi, Manoj;
Chowdhary, Meenakshi;
Mehta, Anurag

Publication type:

Article

Outcomes of retesting BRCA negative patients using multigene panels.

Published in:

Familial Cancer, 2017, v. 16, n. 3, p. 319, doi. 10.1007/s10689-016-9956-7

By:

Yadav, Siddhartha;
Reeves, Ashley;
Campian, Sarah;
Paine, Amy;
Zakalik, Dana

Publication type:

Article

The hereditary nature of small cell carcinoma of the ovary, hypercalcemic type: two new familial cases.

Published in:

Familial Cancer, 2017, v. 16, n. 3, p. 395, doi. 10.1007/s10689-016-9957-6

By:

Witkowski, Leora;
Donini, Nancy;
Byler-Dann, Rebecca;
Knost, James;
Albrecht, Steffen;
Berchuck, Andrew;
McCluggage, W. Glenn;
Hasselblatt, Martin;
Foulkes, William

Publication type:

Article

Embryonal rhabdomyosarcoma in a patient with a heterozygous frameshift variant in the DICER1 gene and additional manifestations of the DICER1 syndrome.

Published in:

Familial Cancer, 2017, v. 16, n. 3, p. 401, doi. 10.1007/s10689-016-9958-5

By:

Fremerey, Julia;
Balzer, Stefan;
Brozou, Triantafyllia;
Schaper, Joerg;
Borkhardt, Arndt;
Kuhlen, Michaela

Publication type:

Article

ATM mutations for surgeons.

Published in:

Familial Cancer, 2017, v. 16, n. 3, p. 407, doi. 10.1007/s10689-016-9959-4

By:

Mansfield, Sara;
Pilarski, Robert;
Agnese, Doreen

Publication type:

Article

Identification of MSH2 inversion of exons 1-7 in clinical evaluation of families with suspected Lynch syndrome.

Published in:

Familial Cancer, 2017, v. 16, n. 3, p. 357, doi. 10.1007/s10689-016-9960-y

By:

Mork, Maureen;
Rodriguez, Andrea;
Taggart, Melissa;
Rodriguez-Bigas, Miguel;
Lynch, Patrick;
Bannon, Sarah;
You, Y.;
Vilar, Eduardo

Publication type:

Article

Mutation screening of ACKR3 and COPS8 in kidney cancer cases from the CONFIRM study.

Published in:

Familial Cancer, 2017, v. 16, n. 3, p. 411, doi. 10.1007/s10689-016-9961-x

By:

Mahmoodi, Maryam;
Nguyen-Dumont, Tu;
Hammet, Fleur;
Pope, Bernard;
Park, Daniel;
Southey, Melissa;
Darlow, John;
Bruinsma, Fiona;
Winship, Ingrid

Publication type:

Article

Novel and reported pathogenic variants in exon 11 of BRCA2 gene in a cohort of Sri Lankan young breast cancer patients.

Published in:

Familial Cancer, 2017, v. 16, n. 3, p. 329, doi. 10.1007/s10689-016-9962-9

By:

Silva, Sumadee;
Tennekoon, Kamani;
Dissanayake, Aravinda;
Silva, Kanishka;
Jayasekara, Lakshika

Publication type:

Article

Psychosocial morbidity in TP53 mutation carriers: is whole-body cancer screening beneficial?

Published in:

Familial Cancer, 2017, v. 16, n. 3, p. 423, doi. 10.1007/s10689-016-9964-7

By:

McBride, Kate;
Ballinger, Mandy;
Schlub, Timothy;
Young, Mary-Anne;
Tattersall, Martin;
Kirk, Judy;
Eeles, Ros;
Killick, Emma;
Walker, Leslie;
Shanley, Sue;
Thomas, David;
Mitchell, Gillian

Publication type:

Article

Baseline results from the UK SIGNIFY study: a whole-body MRI screening study in TP53 mutation carriers and matched controls.

Published in:

Familial Cancer, 2017, v. 16, n. 3, p. 433, doi. 10.1007/s10689-017-9965-1

By:

Saya, Sibel;
Killick, Emma;
Thomas, Sarah;
Taylor, Natalie;
Bancroft, Elizabeth;
Rothwell, Jeanette;
Benafif, Sarah;
Dias, Alexander;
Mikropoulos, Christos;
Pope, Jenny;
Chamberlain, Anthony;
Gunapala, Ranga;
Izatt, Louise;
Side, Lucy;
Walker, Lisa;
Tomkins, Susan;
Cook, Jackie;
Barwell, Julian;
Wiles, Vicki;
Limb, Lauren

Publication type:

Article

Patients with negative multi-gene panel testing: a back to the future paradox?

Published in:

2017

By:

Sorscher, Steven

Publication type:

Letter

Gastric tumours in FAP.

Published in:

Familial Cancer, 2017, v. 16, n. 3, p. 363, doi. 10.1007/s10689-017-9966-0

By:

Walton, Sarah-Jane;
Frayling, Ian;
Clark, Susan;
Latchford, Andrew

Publication type:

Article

Biallelic BRCA2 mutations in two black South African children with Fanconi anaemia.

Published in:

Familial Cancer, 2017, v. 16, n. 3, p. 441, doi. 10.1007/s10689-017-9968-y

By:

Feben, Candice;
Spencer, Careni;
Lochan, Anneline;
Laing, Nakita;
Fieggen, Karen;
Honey, Engela;
Wainstein, Tasha;
Krause, Amanda

Publication type:

Article

A lesson from a reported pathogenic variant in Peutz-Jeghers syndrome: a case report.

Published in:

Familial Cancer, 2017, v. 16, n. 3, p. 417, doi. 10.1007/s10689-016-9963-8

By:

Tan, Hu;
Wei, Xianda;
Yang, Pu;
Huang, Yanru;
Li, Haoxian;
Liang, Desheng;
Wu, Lingqian

Publication type:

Article

Supporting disclosure of genetic information to family members: professional practice and timelines in cancer genetics.

Published in:

Familial Cancer, 2017, v. 16, n. 3, p. 447, doi. 10.1007/s10689-017-9970-4

By:

Derbez, Benjamin;
Pauw, Antoine;
Stoppa-Lyonnet, Dominique;
Montgolfier, Sandrine

Publication type:

Article

The association between prognosis of breast cancer and first-degree family history of breast or ovarian cancer: a systematic review and meta-analysis.

Published in:

Familial Cancer, 2017, v. 16, n. 3, p. 339, doi. 10.1007/s10689-017-9969-x

By:

Song, Jun-Long;
Chen, Chuang;
Yuan, Jing-Ping;
Sun, Sheng-Rong

Publication type:

Article

Identification of a rare germline NBN gene mutation by whole exome sequencing in a lung-cancer survivor from a large family with various types of cancer.

Published in:

Familial Cancer, 2017, v. 16, n. 3, p. 389, doi. 10.1007/s10689-016-9954-9

By:

Marafie, Makia;
Dashti, Mohammed;
Al-Mulla, Fahd

Publication type:

Article

Gastric cancer in FAP: a concerning rise in incidence.

Published in:

Familial Cancer, 2017, v. 16, n. 3, p. 371, doi. 10.1007/s10689-017-9971-3

By:

Mankaney, Gautam;
Leone, Pamela;
Cruise, Michael;
LaGuardia, Lisa;
O'Malley, Margaret;
Bhatt, Amit;
Church, James;
Burke, Carol

Publication type:

Article

Universal screening for Lynch syndrome among patients with colorectal cancer: patient perspectives on screening and sharing results with at-risk relatives.

Published in:

Familial Cancer, 2017, v. 16, n. 3, p. 377, doi. 10.1007/s10689-017-9972-2

By:

Hunter, Jessica;
Arnold, Kathleen;
Cook, Jennifer;
Zepp, Jamilyn;
Gilmore, Marian;
Rope, Alan;
Davis, James;
Bergen, Kellene;
Esterberg, Elizabeth;
Muessig, Kristin;
Peterson, Susan;
Syngal, Sapna;
Acheson, Louise;
Wiesner, Georgia;
Reiss, Jacob;
Goddard, Katrina

Publication type:

Article

Correlation between germline mutations in MMR genes and microsatellite instability in ovarian cancer specimens.

Published in:

Familial Cancer, 2017, v. 16, n. 3, p. 351, doi. 10.1007/s10689-017-9973-1

By:

Akbari, Mohammad;
Zhang, Shiyu;
Cragun, Deborah;
Lee, Ji-Hyun;
Coppola, Domenico;
McLaughlin, John;
Risch, Harvey;
Rosen, Barry;
Shaw, Patricia;
Sellers, Thomas;
Schildkraut, Joellen;
Narod, Steven;
Pal, Tuya

Publication type:

Article