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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2014 1
2015 2
2016 2
2017 1
2018 1
2019 2
2020 1
2023 1
2024 0

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9 results

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Page 1
Preimplantation genetic testing and child health: a national register-based study.
Ginström Ernstad E, Hanson C, Wånggren K, Thurin-Kjellberg A, Hulthe Söderberg C, Syk Lundberg E, Petzold M, Wennerholm UB, Bergh C. Ginström Ernstad E, et al. Among authors: syk lundberg e. Hum Reprod. 2023 Apr 3;38(4):739-750. doi: 10.1093/humrep/dead021. Hum Reprod. 2023. PMID: 36749096 Free PMC article.
Ataxia in Patients With Bi-Allelic NFASC Mutations and Absence of Full-Length NF186.
Kvarnung M, Shahsavani M, Taylan F, Moslem M, Breeuwsma N, Laan L, Schuster J, Jin Z, Nilsson D, Lieden A, Anderlid BM, Nordenskjöld M, Syk Lundberg E, Birnir B, Dahl N, Nordgren A, Lindstrand A, Falk A. Kvarnung M, et al. Among authors: syk lundberg e. Front Genet. 2019 Sep 24;10:896. doi: 10.3389/fgene.2019.00896. eCollection 2019. Front Genet. 2019. PMID: 31608123 Free PMC article.
CTNND2-a candidate gene for reading problems and mild intellectual disability.
Hofmeister W, Nilsson D, Topa A, Anderlid BM, Darki F, Matsson H, Tapia Páez I, Klingberg T, Samuelsson L, Wirta V, Vezzi F, Kere J, Nordenskjöld M, Syk Lundberg E, Lindstrand A. Hofmeister W, et al. Among authors: syk lundberg e. J Med Genet. 2015 Feb;52(2):111-22. doi: 10.1136/jmedgenet-2014-102757. Epub 2014 Dec 3. J Med Genet. 2015. PMID: 25473103