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Results by year

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

Year Number of Results
1969 1
1974 3
1980 6
1981 7
1982 6
1983 3
1984 4
1985 7
1986 2
1987 4
1988 10
1989 9
1990 11
1991 7
1992 1
1993 12
1994 12
1995 15
1996 15
1997 17
1998 13
1999 13
2000 15
2001 10
2002 7
2003 13
2004 8
2005 20
2006 15
2007 12
2008 25
2009 9
2010 22
2011 20
2012 16
2013 19
2014 21
2015 14
2016 11
2017 15
2018 13
2019 17
2020 20
2021 16
2022 14
2023 11
2024 4

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PubMed for id: 867041

500 results

Results by year

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Page 1
A Recurrent Nonsense Mutation in NECTIN4 Underlying Ectodermal Dysplasia-Syndactyly Syndrome with a Novel Phenotype in a Consanguineous Kashmiri Family.
Ali G, Sadia S, Ain-Ul-Batool S, Azeem Z, Awan NB, Kazmi SAR, Ur-Rehman Z, Anjum Z, Ur-Rehman F, Wali A, Khan K, Zaman N, Ayub M, Sajid M, Hassan N. Ali G, et al. Genet Res (Camb). 2023 Oct 4;2023:9999660. doi: 10.1155/2023/9999660. eCollection 2023. Genet Res (Camb). 2023. PMID: 37829154 Free PMC article.
Variants in EFCAB7 underlie nonsyndromic postaxial polydactyly.
Bilal M, Khan H, Khan MJ, Haack TB, Buchert R, Liaqat K, Ullah K, Ahmed S, Bharadwaj T, Acharya A, Peralta S, Najumuddin, Ali H, Hasni MS, Schrauwen I, Ullah A, Ahmad W, Leal SM. Bilal M, et al. Eur J Hum Genet. 2023 Nov;31(11):1270-1274. doi: 10.1038/s41431-023-01450-5. Epub 2023 Sep 8. Eur J Hum Genet. 2023. PMID: 37684519
500 results