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Results by year

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

Year Number of Results
1980 1
1981 1
1983 1
1985 1
1988 1
1989 1
1992 2
1993 1
1994 2
1996 1
1997 7
1998 3
1999 1
2000 3
2001 4
2002 5
2003 3
2004 6
2005 6
2006 1
2007 7
2008 5
2009 5
2010 3
2011 8
2012 7
2013 3
2014 1
2015 3
2016 1
2017 4
2018 5
2019 3
2020 2
2021 4
2022 5
2023 1
2024 1

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PubMed for id: 869741

107 results

Results by year

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Page 1
Novel Pathogenetic Variants in PTHLH and TRPS1 Genes Causing Syndromic Brachydactyly.
Elli FM, Mattinzoli D, Lucca C, Piu M, Maffini MA, Costanza J, Fontana L, Santaniello C, Forino C, Milani D, Bonati MT, Secco A, Gastaldi R, Alfieri C, Messa P, Miozzo M, Arosio M, Mantovani G. Elli FM, et al. J Bone Miner Res. 2022 Mar;37(3):465-474. doi: 10.1002/jbmr.4490. Epub 2022 Jan 17. J Bone Miner Res. 2022. PMID: 34897794 Free PMC article.
Approach to inherited hypertrichosis: A brief review.
Buch J, Ranganath P. Buch J, et al. Indian J Dermatol Venereol Leprol. 2021 Jan-Feb;88(1):11-21. doi: 10.25259/IJDVL_629_20. Indian J Dermatol Venereol Leprol. 2021. PMID: 34379956 Free article. Review.
Oliver McFarlane syndrome: two new cases and a review of the literature.
Lisbjerg K, Andersen MKG, Bertelsen M, Brost AG, Buchvald FF, Jensen RB, Bisgaard AM, Rosenberg T, Tümer Z, Kessel L. Lisbjerg K, et al. Ophthalmic Genet. 2021 Aug;42(4):464-473. doi: 10.1080/13816810.2021.1904419. Epub 2021 Apr 5. Ophthalmic Genet. 2021. PMID: 33818269 Review.
107 results