Skip NavigationSkip to Content

NCI at Frederick Scientific Publications Advanced Search

Search

  1. NCI-F Publications

  2. Return to Quick Search
Search
  2. Year Published:

Your search returned 5 results.
User Information
Export Records
  1. 1.   Standards for the classification of pathogenicity of somatic variants in cancer (oncogenicity): Joint recommendations of Clinical Genome Resource (ClinGen), Cancer Genomics Consortium (CGC), and Variant Interpretation for Cancer Consortium (VICC)
  2. Horak, Peter; Griffith, Malachi; Danos, Arpad M; Pitel, Beth A; Madhavan, Subha; Liu, Xuelu; Chow, Cynthia; Williams, Heather; Carmody, Leigh; Barrow-Laing, Lisa; Rieke, Damian; Kreutzfeldt, Simon; Stenzinger, Albrecht; Tamborero, David; Benary, Manuela; Rajagopal, Padma Sheila; Ida, Cristiane M; Lesmana, Harry; Satgunaseelan, Laveniya; Merker, Jason D; Tolstorukov, Michael Y; Campregher, Paulo Vidal; Warner, Jeremy L; Rao, Shruti; Natesan, Maya; Shen, Haolin; Venstrom, Jeffrey; Roy, Somak; Tao, Kayoko; Kanagal-Shamanna, Rashmi; Xu, Xinjie; Ritter, Deborah I; Pagel, Kym; Krysiak, Kilannin; Dubuc, Adrian; Akkari, Yassmine M; Li, Xuan Shirley; Lee, Jennifer; King, Ian; Raca, Gordana; Wagner, Alex H; Li, Marylin M; Plon, Sharon E; Kulkarni, Shashikant; Griffith, Obi L; Chakravarty, Debyani; Sonkin, Dmitriy
  3. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 2022, Jan 28;
  1. 2.   A germline 1;3 translocation disrupting the VHL gene: a novel genetic cause for von Hippel-Lindau
  2. Ricketts, Christopher J; Vocke, Cathy D; Lang, Martin; Chen,Jack; Zhao,Yongmei; Tran,Bao; Tandon, Mayank; Schmidt, Laura S; Ball, Mark W; Linehan, W Marston
  3. Journal of Medical Genetics. 2022, Jan; 59(1): 18-22.
  1. 3.   Genotype-cancer association in patients with Fanconi anemia due to pathogenic variants in FANCD1 (BRCA2) or FANCN (PALB2)
  2. McReynolds, Lisa J.; Biswas,Kajal; Giri, Neelam; Sharan, Shyam K.; Alter, Blanche P.
  3. Cancer Genetics. 2021, Oct 04; 258-259: 101-109.
  1. 4.   The causes of Fanconi anemia in South Asia and the Middle East: A case series and review of the literature
  2. Thompson, Ashley S; Saba, Nusrat; McReynolds, Lisa J; Munir, Saeeda; Ahmed, Parvez; Sajjad, Sumaira; Jones,Kristine; Yeager,Meredith; Donovan, Frank X; Chandrasekharappa, Settara C; Alter, Blanche P; Savage, Sharon A; Rehman, Sadia
  3. Molecular genetics & genomic medicine. 2021, May 07; e1693.
  1. 5.   Genetic Testing for APOL1 Genetic Variants in Clinical Practice: Finally Starting to Arrive
  2. Kopp, Jeffrey B; Winkler,Cheryl
  3. Clinical journal of the American Society of Nephrology : CJASN. 2020, JAN 7; 15(1): 126-128.
NCI at Frederick

You are leaving a government website.

This external link provides additional information that is consistent with the intended purpose of this site. The government cannot attest to the accuracy of a non-federal site.

Linking to a non-federal site does not constitute an endorsement by this institution or any of its employees of the sponsors or the information and products presented on the site. You will be subject to the destination site's privacy policy when you follow the link.

ContinueCancel