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

Year Number of Results
2002 12
2003 17
2004 10
2005 18
2006 12
2007 19
2008 20
2009 25
2010 37
2011 21
2012 26
2013 24
2014 32
2015 39
2016 28
2017 26
2018 34
2019 35
2020 35
2021 38
2022 30
2023 22
2024 13

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528 results

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Page 1
Joubert syndrome: Molecular basis and treatment.
Spahiu L, Behluli E, Grajçevci-Uka V, Liehr T, Temaj G. Spahiu L, et al. Among authors: liehr t. J Mother Child. 2023 Feb 22;26(1):118-123. doi: 10.34763/jmotherandchild.20222601.d-22-00034. eCollection 2022 Mar 1. J Mother Child. 2023. PMID: 36803942 Free PMC article. Review.
Mucopolysaccharidosis III: Molecular basis and treatment.
Spahiu L, Behluli E, Peterlin B, Nefic H, Hadziselimovic R, Liehr T, Temaj G. Spahiu L, et al. Among authors: liehr t. Pediatr Endocrinol Diabetes Metab. 2021;27(3):201-208. doi: 10.5114/pedm.2021.109270. Pediatr Endocrinol Diabetes Metab. 2021. PMID: 34743503 Free PMC article. Review.
Recommendations for whole genome sequencing in diagnostics for rare diseases.
Souche E, Beltran S, Brosens E, Belmont JW, Fossum M, Riess O, Gilissen C, Ardeshirdavani A, Houge G, van Gijn M, Clayton-Smith J, Synofzik M, de Leeuw N, Deans ZC, Dincer Y, Eck SH, van der Crabben S, Balasubramanian M, Graessner H, Sturm M, Firth H, Ferlini A, Nabbout R, De Baere E, Liehr T, Macek M, Matthijs G, Scheffer H, Bauer P, Yntema HG, Weiss MM. Souche E, et al. Among authors: liehr t. Eur J Hum Genet. 2022 Sep;30(9):1017-1021. doi: 10.1038/s41431-022-01113-x. Epub 2022 May 16. Eur J Hum Genet. 2022. PMID: 35577938 Free PMC article.
Preface.
Trifonov VA, Cioffi MB, Liehr T. Trifonov VA, et al. Among authors: liehr t. Cytogenet Genome Res. 2021;161(1-2):5. doi: 10.1159/000513608. Epub 2021 Apr 22. Cytogenet Genome Res. 2021. PMID: 33887739 Free article. No abstract available.
Repetitive Elements in Humans.
Liehr T. Liehr T. Int J Mol Sci. 2021 Feb 19;22(4):2072. doi: 10.3390/ijms22042072. Int J Mol Sci. 2021. PMID: 33669810 Free PMC article. Review.
Non-Invasive Prenatal Testing in Germany.
Liehr T, Harutyunyan T, Williams H, Weise A. Liehr T, et al. Diagnostics (Basel). 2022 Nov 16;12(11):2816. doi: 10.3390/diagnostics12112816. Diagnostics (Basel). 2022. PMID: 36428876 Free PMC article. Review.
Microdeletion and microduplication syndromes.
Weise A, Mrasek K, Klein E, Mulatinho M, Llerena JC Jr, Hardekopf D, Pekova S, Bhatt S, Kosyakova N, Liehr T. Weise A, et al. Among authors: liehr t. J Histochem Cytochem. 2012 May;60(5):346-58. doi: 10.1369/0022155412440001. Epub 2012 Mar 6. J Histochem Cytochem. 2012. PMID: 22396478 Free PMC article. Review.
528 results