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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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2013 | 1 |
2020 | 1 |
2021 | 1 |
2024 | 0 |
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Floppy infant syndrome as a first manifestation of LMNA-related congenital muscular dystrophy.
Eur J Paediatr Neurol. 2021 May;32:115-121. doi: 10.1016/j.ejpn.2021.04.005. Epub 2021 Apr 20.
Eur J Paediatr Neurol. 2021.
PMID: 33940562
A Rare Mutation in The APOB Gene Associated with Neurological Manifestations in Familial Hypobetalipoproteinemia.
Musialik J, Boguszewska-Chachulska A, Pojda-Wilczek D, Gorzkowska A, Szymańczak R, Kania M, Kujawa-Szewieczek A, Wojcieszyn M, Hartleb M, Więcek A.
Musialik J, et al. Among authors: szymanczak r.
Int J Mol Sci. 2020 Feb 20;21(4):1439. doi: 10.3390/ijms21041439.
Int J Mol Sci. 2020.
PMID: 32093271
Free PMC article.
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Identification and characterization of the first microsatellite loci for the thick-shelled river mussel Unio crassus (Bivalvia: Unionidae).
Sell J, Mioduchowska M, Kaczmarczyk A, Szymańczak R.
Sell J, et al. Among authors: szymanczak r.
J Exp Zool A Ecol Genet Physiol. 2013 Feb;319(2):113-6. doi: 10.1002/jez.1778. Epub 2013 Jan 11.
J Exp Zool A Ecol Genet Physiol. 2013.
PMID: 23315817
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