Works matching IS 13899600 AND DT 2022 AND VI 21 AND IP 1

Results: 14

Use of sanger and next-generation sequencing to screen for mosaic and intronic APC variants in unexplained colorectal polyposis patients.

Published in:

Familial Cancer, 2022, v. 21, n. 1, p. 79, doi. 10.1007/s10689-021-00236-2

By:

Elsayed, Fadwa A.;
Tops, Carli M. J.;
Nielsen, Maartje;
Morreau, Hans;
Hes, Frederik J.;
van Wezel, Tom

Publication type:

Article

Correction to: Infantile fibrosarcoma with TPN3-NTRK3 fusion in a boy with Bloom Syndrome.

Published in:

Familial Cancer, 2022, v. 21, n. 1, p. 91, doi. 10.1007/s10689-020-00223-z

By:

Huson, Sue M.;
Staab, Timo;
Pereira, Marta;
Ward, Heather;
Paredes, Roberto;
Evans, D. Gareth;
Baumhoer, Daniel;
O'Sullivan, James;
Cheesman, Ed;
Schindler, Detlev;
Meyer, Stefan

Publication type:

Article

Knowledge and psychosocial impact of genetic counseling and multigene panel testing among individuals with ovarian cancer.

Published in:

Familial Cancer, 2022, v. 21, n. 1, p. 35, doi. 10.1007/s10689-021-00240-6

By:

Pozzar, Rachel A.;
Hong, Fangxin;
Xiong, Niya;
Stopfer, Jill E.;
Nayak, Manan M.;
Underhill-Blazey, Meghan

Publication type:

Article

Age of diagnosis in familial Barrett's associated neoplasia.

Published in:

Familial Cancer, 2022, v. 21, n. 1, p. 115, doi. 10.1007/s10689-021-00239-z

By:

Glamour, Benita K.;
Alaber, Omar;
Cioffi, Gino;
Chandar, Apoorva K.;
Barnholtz-Sloan, Jill;
Brock, Wendy;
Falk, Gary W.;
Canto, Marcia I.;
Wang, Jean S.;
Iyer, Prasad G.;
Shaheen, Nicholas J.;
Grady, William M.;
Abrams, Julian A.;
Thota, Prashanthi N.;
Chak, Amitabh;
Blum, Andrew E.

Publication type:

Article

Managing gastric cancer risk in lynch syndrome: controversies and recommendations.

Published in:

Familial Cancer, 2022, v. 21, n. 1, p. 75, doi. 10.1007/s10689-021-00235-3

By:

Boland, C. Richard;
Yurgelun, Matthew B.;
Mraz, Kathryn A.;
Boland, Patrick M.

Publication type:

Article

The needs of Southeast Asian BRCA mutation carriers considering risk-reducing salpingo-oophorectomy: a qualitative study.

Published in:

Familial Cancer, 2022, v. 21, n. 1, p. 21, doi. 10.1007/s10689-021-00232-6

By:

Sa'at, Hamizah;
Lee, Yew-Kong;
Yoon, Sook-Yee;
Wong, Siu Wan;
Woo, Yin Ling;
Barlow-Stewart, Kristine;
Mohd Taib, Nur Aishah

Publication type:

Article

Approach to screening for Familial Adenomatous Polyposis (FAP) in a cohort of 226 patients with Desmoid-type Fibromatosis (DF): experience of a specialist center in the UK.

Published in:

Familial Cancer, 2022, v. 21, n. 1, p. 69, doi. 10.1007/s10689-021-00230-8

By:

Cojocaru, E.;
Gennatas, S.;
Thway, K.;
Fisher, C.;
Smrke, A.;
Strauss, D.;
Hayes, A.;
Smith, M.;
Jones, R. L.;
Benson, C.;
McVeigh, T. P.

Publication type:

Article

Genetic predisposition to prostate cancer: an update.

Published in:

Familial Cancer, 2022, v. 21, n. 1, p. 101, doi. 10.1007/s10689-021-00227-3

By:

Ni Raghallaigh, Holly;
Eeles, Rosalind

Publication type:

Article

Comparison of universal screening in major lynch-associated tumors: a systematic review of literature.

Published in:

Familial Cancer, 2022, v. 21, n. 1, p. 57, doi. 10.1007/s10689-020-00226-w

By:

Kunnackal John, George;
Das Villgran, Vipin;
Caufield-Noll, Christine;
Giardiello, Francis M.

Publication type:

Article

Progress Report: New insights into the prevention of CRC by colonoscopic surveillance in Lynch syndrome.

Published in:

Familial Cancer, 2022, v. 21, n. 1, p. 49, doi. 10.1007/s10689-020-00225-x

By:

Vasen, Hans F. A.

Publication type:

Article

Interpretation of BRCA2 Splicing Variants: A Case Series of Challenging Variant Interpretations and the Importance of Functional RNA Analysis.

Published in:

Familial Cancer, 2022, v. 21, n. 1, p. 7, doi. 10.1007/s10689-020-00224-y

By:

Nix, Paola;
Mundt, Erin;
Coffee, Bradford;
Goossen, Elizabeth;
Warf, Bryan M.;
Brown, Krystal;
Bowles, Karla;
Roa, Benjamin

Publication type:

Article

Genetic evaluation of patients and families with concern for hereditary endocrine tumor syndromes.

Published in:

Familial Cancer, 2022, v. 21, n. 1, p. 93, doi. 10.1007/s10689-020-00222-0

By:

Anderson, Jennifer L.;
Pilarski, Robert;
Kirschner, Lawrence;
Brock, Pamela

Publication type:

Article

Infantile fibrosarcoma with TPM3-NTRK1 fusion in a boy with Bloom syndrome.

Published in:

2022

By:

Huson, Sue M.;
Staab, Timo;
Pereira, Marta;
Ward, Heather;
Paredes, Roberto;
Evans, D. Gareth;
Baumhoer, Daniel;
O'Sullivan, James;
Cheesman, Ed;
Schindler, Detlev;
Meyer, Stefan

Publication type:

Case Study

Atypical choroidal nevus in a subject with a germline PALB2 pathogenic variant.

Published in:

2022

By:

Grosel, Timothy W.;
Karl, Matthew;
Pilarski, Robert T.;
Davidorf, Frederick H.;
Abdel-Rahman, Mohamed H.;
Cebulla, Colleen M.

Publication type:

Case Study