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NARA Subscribed4
Publisher
Springer Nature4
Journal
Familial Cancer3
Human Genetics1
Publication Year
20111
20091
20051
20031
Reetta Kariola results 4 · Newest (Page 1/1, per page 25)
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A putative Lynch syndrome family carrying MSH2 and MSH6 variants of uncertain significance—functional analysis reveals the pathogenic oneNARA Subscribed
Familial Cancer · 2011 · Vol. 10 · Issue 3 · Springer
Jukka Kantelinen; Thomas v. O. Hansen; Minttu Kansikas; Lotte Nylandsted Krogh; Mari K. Korhonen; Saara Ollila; Minna Nyström; Anne-Marie Gerdes; Reetta Kariola
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Functional characterization of rare missense mutations in MLH1 and MSH2 identified in Danish colorectal cancer patientsNARA Subscribed
Familial Cancer · 2009 · Vol. 8 · Issue 4 · Springer
Lise Lotte Christensen; Reetta Kariola; Mari K. Korhonen; Friedrik P. Wikman; Lone Sunde; Anne-Marie Gerdes; Henrik Okkels; Carsten A. Brandt; Inge Bernstein; Thomas V. O. Hansen; Rikke Hagemann-Madsen; Claus L. Andersen; Minna Nyström; Torben F. Ørntoft
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APC and β-catenin protein expression patterns in HNPCC-related endometrial and colorectal cancersNARA Subscribed
Familial Cancer · 2005 · Vol. 4 · Issue 2 · Springer
Reetta Kariola; Wael M. Abdel-Rahman; Miina Ollikainen; Ralf Butzow; Päivi Peltomäki; Minna Nyström
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Two mismatch repair gene mutations found in a colon cancer patient – which one is pathogenic?NARA Subscribed
Human Genetics · 2003 · Vol. 112 · Issue 2 · Springer
Reetta Kariola; Robyn Otway; Karin E. Lönnqvist; Tiina E. Raevaara; Finlay Macrae; Yvonne J. Vos; Maija Kohonen-Corish; Robert M. Hofstra; Minna Nyström-Lahti
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