학술논문
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Pal Møller; Toni T. Seppälä; Aysel Ahadova; Emma J. Crosbie; Elke Holinski-Feder; Rodney Scott; Saskia Haupt; Gabriela Möslein; Ingrid Winship; Sanne W. Bajwa-ten Broeke; Kelly E. Kohut; Neil Ryan; Peter Bauerfeind; Laura E. Thomas; D. Gareth Evans; Stefan Aretz; Rolf H. Sijmons; Elizabeth Half; Karl Heinimann; Karoline Horisberger; Kevin Monahan; Christoph Engel; Giulia Martina Cavestro; Robert Fruscio; Naim Abu-Freha; Levi Zohar; Luigi Laghi; Lucio Bertario; Bernardo Bonanni; Maria Grazia Tibiletti; Leonardo S. Lino-Silva; Carlos Vaccaro; Adriana Della Valle; Benedito Mauro Rossi; Leandro Apolinário da Silva; Ivana Lucia de Oliveira Nascimento; Norma Teresa Rossi; Tadeusz Dębniak; Jukka-Pekka Mecklin; Inge Bernstein; Annika Lindblom; Lone Sunde; Sigve Nakken; Vincent Heuveline; John Burn; Eivind Hovig; Matthias Kloor; Julian R. Sampson; Mev Dominguez-Valentin; On behalf of the Prospective Lynch Syndrome Database (www.plsd.eu) and The European Hereditary Tumour Group (www.ehtg.org)
Hereditary Cancer in Clinical Practice, Vol 21, Iss 1, Pp 1-12 (2023)
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[AR] Kelly E. Kohut
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