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Mosaics and moles.
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Myoblasts generated by lentiviral mediated MyoD transduction of myotonic dystrophy type 1 (DM1) fibroblasts can be used for assays of therapeutic molecules.
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Paediatric B-cell precursor acute lymphoblastic leukaemia with t(1;19)(q23;p13): Clinical and cytogenetic characteristics of 47 cases from the Nordic countries treated according to NOPHO protocols.
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Prenatal diagnostics of a DYNC2H1 deletion and a point mutation as a cause of Asphyxiating Thoracic Dysplasia. Abstract from 7th International DECIPHER Symposium , Hinxton, United Kingdom.
Christensen, R., Owens, D. M.
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Aarskog-Scott syndrome: Clinical update and report of nine novel mutations of the FGD1 gene.
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Common Breast Cancer Susceptibility Alleles and the Risk of Breast Cancer for BRCA1 and BRCA2 Mutation Carriers: Implications for Risk Prediction.
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Escherichia coli α-hemolysin triggers shrinkage of erythrocytes via KCa3.1 and TMEM16A channels with subsequent phosphatidylserine exposure.
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Identification of epidermal progenitors for the Merkel cell lineage.
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Increased number of sex chromosomes affects height in a nonlinear fashion: a study of 305 patients with sex chromosome aneuploidy.
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Maintenance treatment with azacytidine for patients with high-risk myelodysplastic syndromes (MDS) or acute myeloid leukaemia following MDS in complete remission after induction chemotherapy.
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Recurrence of discordant congenital heart defects in families.
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Systematic medication review and health-related outcome in elderly patients acutely admitted to an orthopaedic ward: a randomised controlled study. Poster session presented at Danish Society for Emergency Medicine: Research Symposium 2010, Denmark.
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Bendix, L.
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The load of short telomeres, estimated by a new method, Universal STELA, correlates with number of senescent cells.
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Functional characterization of rare missense mutations in MLH1 and MSH2 identified in Danish colorectal cancer patients.
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Mismatch repair defective breast cancer in the hereditary nonpolyposis colorectal cancer syndrome.
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Pallister-Killian syndrome in a girl with mild developmental delay and mosaicism for hexasomy 12p.
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Pre-screening HIV-1 reverse transcriptase resistance mutations in subtype B patients using a novel multiplex primer extension assay.
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Zangenberg, M.
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The combined expression of HOXA4 and MEIS1 is an independent prognostic factor in patients with AML.
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Ank, N., Iversen, M. B., Bartholdy, C., Staeheli, P.
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An Important Role for Type III Interferon (IFN-l/IL-28) in TLR-Induced Antiviral Activity.
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Therkildsen, C., Timshel, S., Nilbert, M. & HNPCC-gruppe: Henrik Okkels og Henrik Krarup, Klinisk Biokemisk Afdeling, Aalborg Sygehus; Friedrik Wikman og Torben F. Ørntoft, Klinisk Biokemisk Afdeling, Århus Universitetshospital, Skejby; Thomas v. O. Hansen og Finn C. Nielsen, Klinisk Biokemisk Afdeling, Rigshospitalet; Marie Luise Bisgaard, Institut for Cellulær og Molekylær Medicin, Københavns Universitet; Inge Bernstein, HNPCC-registret, Gastroenheden, Hvidovre Hospital; Lone Sunde, Klinisk Genetisk Afdeling, Århus Universitetshospital; Anne-Marie Gerdes, Afdeling for Biokemi, Farmakologi og Genetik, Odense Universitetssygehus; Dorthe Crüger, Klinisk Genetisk Afdeling, Vejle Sygehus (2008).
Indsigter og udfordringer i danske Lynch-syndrom-familier.
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170(25), 2252-5.