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Nordling, Margareta
45
results:
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Format
Online (45)
Mediatypes
Articles (Online) (26)
OpenAccess-fulltext (19)
Languages
english (43)
finnish (1)
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1
Gene-specific ACMG/AMP classification criteria for germline..:
Spier, Isabel
;
Yin, Xiaoyu
;
Richardson, Marcy
...
Genetics in Medicine. 26 (2024) 2 - p. 100992 , 2024
Link:
https://doi.org/10.1016/..
?
2
Merged testing for colorectal cancer syndromes and re‐evalu..:
Svensson, Sara
;
Zagoras, Theofanis
;
Aravidis, Christos
...
Genes, Chromosomes and Cancer. 61 (2022) 10 - p. 585-591 , 2022
Link:
https://doi.org/10.1002/..
?
3
Identification of known and novel familial cancer genes in ..:
Helgadottir, Hafdis T.
;
Thutkawkorapin, Jessada
;
Rohlin, Anna
...
International Journal of Cancer. 149 (2021) 3 - p. 627-634 , 2021
Link:
https://doi.org/10.1002/..
?
4
Update on genetic predisposition to colorectal cancer and p..:
Valle, Laura
;
de Voer, Richarda M.
;
Goldberg, Yael
...
Molecular Aspects of Medicine. 69 (2019) - p. 10-26 , 2019
Link:
https://doi.org/10.1016/..
?
5
Biallelic germline nonsense variant of MLH3 underlies polyp..:
Olkinuora, Alisa
;
Nieminen, Taina T.
;
Mårtensson, Emma
...
Genetics in Medicine. 21 (2019) 8 - p. 1868-1873 , 2019
Link:
https://doi.org/10.1038/..
?
6
Expanding the genotype–phenotype spectrum in hereditary col..:
Rohlin, Anna
;
Rambech, Eva
;
Kvist, Anders
...
Familial Cancer. 16 (2016) 2 - p. 195-203 , 2016
Link:
https://doi.org/10.1007/..
?
7
GREM1 and POLE variants in hereditary colorectal cancer syn..:
Rohlin, Anna
;
Eiengård, Frida
;
Lundstam, Ulf
...
Genes, Chromosomes and Cancer. 55 (2015) 1 - p. 95-106 , 2015
Link:
https://doi.org/10.1002/..
?
8
Neurofibromatosis 2 with Limited Phenotype in a Kindred wit..:
Wiklund, Leif
;
Flodin, Anna
;
Zyk-Zackrisson, Karin
..
Neurology. 82 (2014) 10_supplement - p. , 2014
Link:
https://doi.org/10.1212/..
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9
Integrative Genetic Characterization and Phenotype Correlat..:
Crona, Joakim
;
Nordling, Margareta
;
Maharjan, Rajani
...
PLoS ONE. 9 (2014) 1 - p. e86756 , 2014
Link:
https://doi.org/10.1371/..
?
10
Parallel sequencing used in detection of mosaic mutations: ..:
Rohlin, Anna
;
Wernersson, Josephine
;
Engwall, Yvonne
...
Human Mutation. 30 (2009) 6 - p. 1012-1020 , 2009
Link:
https://doi.org/10.1002/..
?
11
No germline mutations in supposed tumour suppressor genes S..:
Bergman, Annika
;
Abel, Frida
;
Behboudi, Afrouz
...
BMC Medical Genetics. 9 (2008) 1 - p. , 2008
Link:
https://doi.org/10.1186/..
?
12
Clinical characterization and the mutation spectrum in Swed..:
Kanter-Smoler, Gunilla
;
Fritzell, Kaisa
;
Rohlin, Anna
...
BMC Medicine. 6 (2008) 1 - p. , 2008
Link:
https://doi.org/10.1186/..
?
13
Genome‐wide linkage scan for breast cancer susceptibility l..:
Bergman, Annika
;
Karlsson, Per
;
Berggren, Jonna
...
Genes, Chromosomes and Cancer. 46 (2006) 3 - p. 302-309 , 2006
Link:
https://doi.org/10.1002/..
?
14
Multiplex ligation-dependent probe amplification improves d..:
Arkblad, Eva L.
;
Darin, Niklas
;
Berg, Kerstin
...
Neuromuscular Disorders. 16 (2006) 12 - p. 830-838 , 2006
Link:
https://doi.org/10.1016/..
?
15
Occurrence of both breast and ovarian cancer in a woman is ..:
Einbeigi, Zakaria
;
Bergman, Annika
;
Meis-Kindblom, Jeanne M.
...
Familial Cancer. 6 (2006) 1 - p. 35-41 , 2006
Link:
https://doi.org/10.1007/..
1-15