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Results by year

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

Year Number of Results
1982 3
1984 2
1985 2
1986 4
1987 1
1988 3
1990 2
1991 3
1992 3
1993 7
1994 2
1995 4
1996 2
1997 2
1998 4
1999 2
2001 3
2002 2
2003 2
2004 2
2005 3
2006 4
2007 4
2008 5
2009 3
2010 4
2011 3
2012 4
2013 6
2014 6
2015 5
2016 11
2017 11
2018 13
2019 11
2020 15
2021 5
2022 14
2023 14
2024 5

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PubMed for id: 934637

170 results

Results by year

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Page 1
Lethal multiple pterygium syndrome in a newborn, a case report.
Sadeghimoghadam P, Shirdel S, Hantoushzadeh S, Hashemi Z, Ghaemi M. Sadeghimoghadam P, et al. Clin Case Rep. 2023 Jul 12;11(7):e7678. doi: 10.1002/ccr3.7678. eCollection 2023 Jul. Clin Case Rep. 2023. PMID: 37448946 Free PMC article.
Lethal Congenital Contracture Syndrome 11: A Case Report and Literature Review.
Potrony M, Borrell A, Masoller N, Nadal A, Rodriguez-Carunchio L, Saez de Gordoa Elizalde K, Quesada-Espinosa JF, Villanueva-Cañas JL, Pauta M, Jodar M, Madrigal I, Badenas C, Alvarez-Mora MI, Rodriguez-Revenga L. Potrony M, et al. J Clin Med. 2022 Jun 21;11(13):3570. doi: 10.3390/jcm11133570. J Clin Med. 2022. PMID: 35806855 Free PMC article.
A CNTNAP1 Missense Variant Is Associated with Canine Laryngeal Paralysis and Polyneuropathy.
Letko A, Minor KM, Friedenberg SG, Shelton GD, Salvador JP, Mandigers PJJ, Leegwater PAJ, Winkler PA, Petersen-Jones SM, Stanley BJ, Ekenstedt KJ, Johnson GS, Hansen L, Jagannathan V, Mickelson JR, Drögemüller C. Letko A, et al. Genes (Basel). 2020 Nov 27;11(12):1426. doi: 10.3390/genes11121426. Genes (Basel). 2020. PMID: 33261176 Free PMC article.
Exome sequencing in Crisponi/cold-induced sweating syndrome-like individuals reveals unpredicted alternative diagnoses.
Angius A, Uva P, Oppo M, Buers I, Persico I, Onano S, Cuccuru G, Van Allen MI, Hulait G, Aubertin G, Muntoni F, Fry AE, Annerén G, Stattin EL, Palomares-Bralo M, Santos-Simarro F, Cucca F, Crisponi G, Rutsch F, Crisponi L. Angius A, et al. Clin Genet. 2019 May;95(5):607-614. doi: 10.1111/cge.13532. Epub 2019 Mar 28. Clin Genet. 2019. PMID: 30859550
170 results