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2014 2
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2021 2
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2023 9

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Page 1
[Telomere biology disorders].
Byrjalsen A, Bygum A, Lautrup CK, Frederiksen AL, Fialla AD, Raaschou-Jensen K, Bendstrup E, Madsen TN, Klarskov M, Jelsig AM. Byrjalsen A, et al. Ugeskr Laeger. 2022 Jul 11;184(28):V03220220. Ugeskr Laeger. 2022. PMID: 35959813 Free article. Review. Danish.
Novel Genetic Causes of Gastrointestinal Polyposis Syndromes.
Jelsig AM, Byrjalsen A, Busk Madsen M, Kuhlmann TP, van Overeem Hansen T, Wadt KAW, Karstensen JG. Jelsig AM, et al. Among authors: byrjalsen a. Appl Clin Genet. 2021 Nov 27;14:455-466. doi: 10.2147/TACG.S295157. eCollection 2021. Appl Clin Genet. 2021. PMID: 34866929 Free PMC article. Review.
Nationwide germline whole genome sequencing of 198 consecutive pediatric cancer patients reveals a high incidence of cancer prone syndromes.
Byrjalsen A, Hansen TVO, Stoltze UK, Mehrjouy MM, Barnkob NM, Hjalgrim LL, Mathiasen R, Lautrup CK, Gregersen PA, Hasle H, Wehner PS, Tuckuviene R, Sackett PW, Laspiur AO, Rossing M, Marvig RL, Tommerup N, Olsen TE, Scheie D, Gupta R, Gerdes AM, Schmiegelow K, Wadt K. Byrjalsen A, et al. PLoS Genet. 2020 Dec 17;16(12):e1009231. doi: 10.1371/journal.pgen.1009231. eCollection 2020 Dec. PLoS Genet. 2020. PMID: 33332384 Free PMC article.
Combinatorial batching of DNA for ultralow-cost detection of pathogenic variants.
Stoltze UK, Hagen CM, van Overeem Hansen T, Byrjalsen A, Gerdes AM, Yakimov V, Rasmussen S, Bækvad-Hansen M, Hougaard DM, Schmiegelow K, Hjalgrim H, Wadt K, Bybjerg-Grauholm J. Stoltze UK, et al. Among authors: byrjalsen a. Genome Med. 2023 Mar 14;15(1):17. doi: 10.1186/s13073-023-01167-6. Genome Med. 2023. PMID: 36918911 Free PMC article.
23 results