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Results by year

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

Year Number of Results
1975 3
1976 1
1977 2
1978 2
1979 3
1980 2
1981 1
1982 2
1985 5
1986 2
1987 3
1988 2
1989 1
1990 1
1992 4
1993 5
1994 2
1995 1
1996 5
1997 1
1998 2
1999 1
2000 2
2001 1
2002 5
2003 2
2004 4
2005 3
2006 7
2007 2
2008 9
2009 5
2010 7
2011 5
2012 10
2013 12
2014 10
2015 7
2016 6
2017 4
2018 15
2019 12
2020 16
2021 15
2022 7
2023 8
2024 3

Text availability

Article attribute

Article type

Publication date

PubMed for id: 332232

193 results

Results by year

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Page 1
3M syndrome: A Tunisian seven-cases series.
Khachnaoui-Zaafrane K, Ouertani I, Zanati A, Kandara H, Maazoul F, Mrad R. Khachnaoui-Zaafrane K, et al. Eur J Med Genet. 2022 Mar;65(3):104448. doi: 10.1016/j.ejmg.2022.104448. Epub 2022 Feb 9. Eur J Med Genet. 2022. PMID: 35150935
Mild phenotype in two siblings with a missense GHR variant.
Sarıkaya Özdemir B, Çetinkaya S, Güleray Lafcı N, Şakar M, Karacan Küçükali G, Elmaoğullari S, Savaş Erdeve Ş. Sarıkaya Özdemir B, et al. J Pediatr Endocrinol Metab. 2021 Jul 1;34(10):1349-1354. doi: 10.1515/jpem-2021-0044. Print 2021 Oct 26. J Pediatr Endocrinol Metab. 2021. PMID: 34218547
193 results