Zobrazeno 1 - 10
of 365
pro vyhledávání: '"Iselius, L."'
Publikováno v:
British Journal of Cancer. 2/1/2001, Vol. 84 Issue 3, p429. 6p.
Publikováno v:
Human Heredity, 1982 Jan 01. 32(2), 76-79.
Externí odkaz:
https://www.jstor.org/stable/45101703
Autor:
Iselius, L.
Publikováno v:
Human Heredity, 1981 Jan 01. 31(4), 222-226.
Externí odkaz:
https://www.jstor.org/stable/45101646
Publikováno v:
Human Heredity, 1981 Jan 01. 31(4), 252-258.
Externí odkaz:
https://www.jstor.org/stable/45101652
Publikováno v:
Human Heredity, 1983 Jan 01. 33(5), 277-286.
Externí odkaz:
https://www.jstor.org/stable/45101773
Autor:
Iselius, L., Gustavson, K.H.
Publikováno v:
Human Heredity, 1984 Jan 01. 34(6), 358-363.
Externí odkaz:
https://www.jstor.org/stable/45102116
Publikováno v:
Human Heredity, 1985 Jan 01. 35(1), 43-52.
Externí odkaz:
https://www.jstor.org/stable/45101866
Publikováno v:
Cephalalgia. Aug96, Vol. 16 Issue 5, p305-309. 5p.
Autor:
Marie Luise Bisgaard, Päivi Peltomäki, Skoglund J, Xiao-Lei Zhou, Iselius L, Jana Vandrovcova, Djureinovic T, Annika Lindblom, Renkonen E
Background: The best known hereditary colorectal cancer syndromes, familial adenomatous polyposis (FAP) and hereditary non-polyposis colorectal cancer (HNPCC), constitute about 2% of all colorectal cancers, and there are at least as many non-FAP, non
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5837811f2a84af3d6e8e2c7b9e9fe43a
https://europepmc.org/articles/PMC2564647/
https://europepmc.org/articles/PMC2564647/
Publikováno v:
Europe PubMed Central
A translocation between the long arms of chromosomes 11 and 22, t(11;22)(q23;q11), is the most frequent constitutional reciprocal translocation in man. This chromosome abnormality has not previously been reported to be associated with an increased ri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::4cf070386d77bee6b86ebc0664e5a6f3
https://europepmc.org/articles/PMC1918254/
https://europepmc.org/articles/PMC1918254/