Works matching IS 13899600 AND DT 2018 AND VI 17 AND IP 2

Results: 20

Immunohistochemical null-phenotype for mismatch repair proteins in colonic carcinoma associated with concurrent <italic>MLH1</italic> hypermethylation and <italic>MSH2</italic> somatic mutations.

Published in:

Familial Cancer, 2018, v. 17, n. 2, p. 225, doi. 10.1007/s10689-017-0031-9

By:

Wang, Tao;
Stadler, Zsofia K.;
Zhang, Liying;
Weiser, Martin R.;
Basturk, Olca;
Hechtman, Jaclyn F.;
Vakiani, Efsevia;
Saltz, Lenard B.;
Klimstra, David S.;
Shia, Jinru

Publication type:

Article

Mutational analysis of the RB1 gene and the inheritance patterns of retinoblastoma in Jordan.

Published in:

Familial Cancer, 2018, v. 17, n. 2, p. 261, doi. 10.1007/s10689-017-0027-5

By:

Yousef, Yacoub A.;
Tbakhi, Abdelghani;
Al-Hussaini, Maysa;
AlNawaiseh, Ibrahim;
Saab, Ala;
Afifi, Amal;
Naji, Maysa;
Mohammad, Mona;
Deebajah, Rasha;
Jaradat, Imad;
Sultan, Iyad;
Mehyar, Mustafa

Publication type:

Article

Pancreatic neuroendocrine tumor in a patient with a <italic>TSC1</italic> variant: case report and review of the literature.

Published in:

Familial Cancer, 2018, v. 17, n. 2, p. 275, doi. 10.1007/s10689-017-0029-3

By:

Mortaji, Parisa;
Morris, Katherine T.;
Samedi, Von;
Eberhardt, Steven;
Ryan, Shawnia

Publication type:

Article

p53 signaling pathway polymorphisms, cancer risk and tumor phenotype in <italic>TP53</italic> R337H mutation carriers.

Published in:

Familial Cancer, 2018, v. 17, n. 2, p. 269, doi. 10.1007/s10689-017-0028-4

By:

Macedo, Gabriel S.;
Vieira, Igor Araujo;
Vianna, Fernanda Salles Luiz;
Alemar, Barbara;
Giacomazzi, Juliana;
Brandalize, Ana Paula Carneiro;
Caleffi, Maira;
Volc, Sahlua Miguel;
de Campos Reis Galvão, Henrique;
Palmero, Edenir Inez;
Achatz, Maria Isabel;
Ashton-Prolla, Patricia

Publication type:

Article

A germline missense mutation in exon 3 of the <italic>MSH2</italic> gene in a Lynch syndrome family: correlation with phenotype and localization assay.

Published in:

Familial Cancer, 2018, v. 17, n. 2, p. 215, doi. 10.1007/s10689-017-0030-x

By:

Bianchi, Francesca;
Maccaroni, Elena;
Belvederesi, Laura;
Brugiati, Cristiana;
Giampieri, Riccardo;
Bini, Federica;
Bracci, Raffaella;
Pagliaretta, Silvia;
Del Prete, Michela;
Piva, Francesco;
Mandolesi, Alessandra;
Scarpelli, Marina;
Berardi, Rossana

Publication type:

Article

Discovery of mutations in homologous recombination genes in African-American women with breast cancer.

Published in:

Familial Cancer, 2018, v. 17, n. 2, p. 187, doi. 10.1007/s10689-017-0036-4

By:

Ding, Yuan Chun;
Adamson, Aaron W.;
Steele, Linda;
Bailis, Adam M.;
John, Esther M.;
Tomlinson, Gail;
Neuhausen, Susan L.

Publication type:

Article

Dental anomalies in pediatric patients with familial adenomatous polyposis.

Published in:

Familial Cancer, 2018, v. 17, n. 2, p. 229, doi. 10.1007/s10689-017-0035-5

By:

Septer, Seth;
Bohaty, Brenda;
Onikul, Robin;
Kumar, Vandana;
Williams, Karen B.;
Attard, Thomas M.;
Friesen, Craig A.;
Friesen, Lynn Roosa

Publication type:

Article

Whole body magnetic resonance imaging (WB-MRI) and brain MRI baseline surveillance in <italic>TP53</italic> germline mutation carriers: experience from the Li-Fraumeni Syndrome Education and Early Detection (LEAD) clinic.

Published in:

Familial Cancer, 2018, v. 17, n. 2, p. 287, doi. 10.1007/s10689-017-0034-6

By:

Bojadzieva, Jasmina;
Amini, Behrang;
Day, Suzanne F.;
Jackson, Tiffiny L.;
Thomas, Parijatham S.;
Willis, Brandy J.;
Throckmorton, Whitney R.;
Daw, Najat C.;
Bevers, Therese B.;
Strong, Louise C.

Publication type:

Article

Cancer patients’ intentions towards receiving unsolicited genetic information obtained using next-generation sequencing.

Published in:

Familial Cancer, 2018, v. 17, n. 2, p. 309, doi. 10.1007/s10689-017-0033-7

By:

Bijlsma, Rhodé M.;
Wessels, Hester;
Wouters, Roel H. P.;
May, Anne M.;
Ausems, Margreet G. E. M.;
Voest, Emile E.;
Bredenoord, Annelien L.

Publication type:

Article

Sporadic endometrial adenocarcinoma with MMR deficiency due to biallelic <italic>MSH2</italic> somatic mutations.

Published in:

Familial Cancer, 2018, v. 17, n. 2, p. 281, doi. 10.1007/s10689-017-0032-8

By:

Buecher, Bruno;
De Pauw, Antoine;
Bazire, Louis;
Houdayer, Claude;
Fievet, Alice;
Moncoutier, Virginie;
Farkhondeh, Fereshteh;
Melaabi, Samia;
Lyonnet, Dominique Stoppa;
Golmard, Lisa

Publication type:

Article

The spectrum of genetic variants in hereditary pancreatic cancer includes Fanconi anemia genes.

Published in:

Familial Cancer, 2018, v. 17, n. 2, p. 235, doi. 10.1007/s10689-017-0019-5

By:

Slavin, Thomas P.;
Neuhausen, Susan L.;
Nehoray, Bita;
Niell-Swiller, Mariana;
Solomon, Ilana;
Rybak, Christina;
Blazer, Kathleen;
Adamson, Aaron;
Yang, Kai;
Sand, Sharon;
Guerrero-Llamas, Nancy;
Castillo, Danielle;
Herzog, Josef;
Wu, Xiwei;
Tao, Shu;
Raja, Shivali;
Chung, Vincent;
Singh, Gagandeep;
Nadesan, Sue;
Brown, Sandra

Publication type:

Article

Remarkable effects of imatinib in a family with young onset gastrointestinal stromal tumors and cutaneous hyperpigmentation associated with a germline <italic>KIT</italic>-Trp557Arg mutation: case report and literature overview.

Published in:

Familial Cancer, 2018, v. 17, n. 2, p. 247, doi. 10.1007/s10689-017-0024-8

By:

Farag, S.;
van der Kolk, L. E.;
van Boven, H. H.;
van Akkooi, A. C. J.;
Beets, G. L.;
Wilmink, J. W.;
Steeghs, N.

Publication type:

Article

Screening for Lynch syndrome in young Saudi colorectal cancer patients using microsatellite instability testing and next generation sequencing.

Published in:

Familial Cancer, 2018, v. 17, n. 2, p. 197, doi. 10.1007/s10689-017-0015-9

By:

Alqahtani, Masood;
Edwards, Caitlin;
Buzzacott, Natasha;
Carpenter, Karen;
Alsaleh, Khalid;
Alsheikh, Abdulmalik;
Abozeed, Waleed;
Mashhour, Miral;
Almousa, Afnan;
Housawi, Yousef;
Al Hawwaj, Shareefa;
Iacopetta, Barry

Publication type:

Article

Novel <italic>BRCA1</italic> splice-site mutation in ovarian cancer patients of Slavic origin.

Published in:

Familial Cancer, 2018, v. 17, n. 2, p. 179, doi. 10.1007/s10689-017-0022-x

By:

Krivokuca, Ana;
Dragos, Vita Setrajcic;
Stamatovic, Ljiljana;
Blatnik, Ana;
Boljevic, Ivana;
Stegel, Vida;
Rakobradovic, Jelena;
Skerl, Petra;
Jovandic, Stevo;
Krajc, Mateja;
Magic, Mirjana Brankovic;
Novakovic, Srdjan

Publication type:

Article

Issues related to family history of cancer at the end of life: a palliative care providers’ survey.

Published in:

Familial Cancer, 2018, v. 17, n. 2, p. 303, doi. 10.1007/s10689-017-0021-y

By:

Gonthier, Catherine;
Pelletier, Sylvie;
Gagnon, Pierre;
Marin, Ana;
Chiquette, Jocelyne;
Gagnon, Bruno;
Roy, Louis;
Cléophat, Jude Emmanuel;
Joly, Yann;
Dorval, Michel

Publication type:

Article

Pancreatic adenocarcinoma with a germline <italic>PTEN</italic> p.Arg234Gln mutation.

Published in:

Familial Cancer, 2018, v. 17, n. 2, p. 255, doi. 10.1007/s10689-017-0025-7

By:

Uemura, Sunao;
Matsubayashi, Hiroyuki;
Kiyozumi, Yoshimi;
Uesaka, Katsuhiko;
Yamamoto, Yusuke;
Sasaki, Keiko;
Abe, Masato;
Urakami, Kenichi;
Kusuhara, Masatoshi;
Yamaguchi, Ken

Publication type:

Article

A new hereditary colorectal cancer network in the Middle East and eastern mediterranean countries to improve care for high-risk families.

Published in:

Familial Cancer, 2018, v. 17, n. 2, p. 209, doi. 10.1007/s10689-017-0018-6

By:

Ghorbanoghli, Zeinab;
Jabari, Carol;
Sweidan, Walid;
Hammoudeh, Wail;
Cortas, George;
Sharara, Ala I.;
Abedrabbo, Amal;
Hourani, Ijad;
Mahjoubi, Bahareh;
Majidzadeh, Keivan;
Tözün, Nurdan;
Ziada-Bouchaar, Hadia;
Hamoudi, Waseem;
Diab, Osama;
Khorshid, Hamid Reza Khorram;
Lynch, Henry;
Vasen, Hans

Publication type:

Article

Erratum to: A new hereditary colorectal cancer network in the Middle East and eastern Mediterranean countries to improve care for high-risk families.

Published in:

Familial Cancer, 2018, v. 17, n. 2, p. 213, doi. 10.1007/s10689-017-0023-9

By:

Ghorbanoghli, Zeinab;
Jabari, Carol;
Sweidan, Walid;
Hammoudeh, Wail;
Cortas, George;
Sharara, Ala I.;
Abedrabbo, Amal;
Hourani, Ijad;
Mahjoubi, Bahareh;
Majidzadeh, Keivan;
Tözün, Nurdan;
Ziada-Bouchaar, Hadia;
Hamoudi, Waseem;
Diab, Osama;
Khorshid, Hamid Reza Khorram;
Lynch, Henry;
Vasen, Hans

Publication type:

Article

A comparison of cosegregation analysis methods for the clinical setting.

Published in:

Familial Cancer, 2018, v. 17, n. 2, p. 295, doi. 10.1007/s10689-017-0017-7

By:

Rañola, John Michael O.;
Liu, Quanhui;
Rosenthal, Elisabeth A.;
Shirts, Brian H.

Publication type:

Article

Screening of <italic>BMPR1a</italic> for pathogenic mutations in familial colorectal cancer type X families from Newfoundland.

Published in:

Familial Cancer, 2018, v. 17, n. 2, p. 205, doi. 10.1007/s10689-017-0016-8

By:

Evans, Daniel R.;
Green, Jane S.;
Woods, Michael O.

Publication type:

Article