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

Year Number of Results
1901 1
1921 1
1939 1
1950 1
1953 1
1960 1
1977 1
1978 1
1979 2
1980 1
1982 1
1984 2
1985 1
1986 1
1987 1
1988 3
1989 2
1990 2
1991 3
1992 1
1993 1
1994 2
1995 1
1996 4
1997 4
1998 1
1999 1
2001 5
2002 2
2004 2
2005 4
2006 3
2007 2
2008 6
2009 4
2010 6
2011 8
2012 8
2013 12
2014 12
2015 10
2016 23
2017 14
2018 21
2019 17
2020 13
2021 8
2022 6
2023 1
2024 0

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Similar articles for PMID: 26710928

205 results

Results by year

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Page 1
Expanding the mutation and clinical spectrum of Roberts syndrome.
Afifi HH, Abdel-Salam GM, Eid MM, Tosson AM, Shousha WG, Abdel Azeem AA, Farag MK, Mehrez MI, Gaber KR. Afifi HH, et al. Congenit Anom (Kyoto). 2016 Jul;56(4):154-62. doi: 10.1111/cga.12151. Congenit Anom (Kyoto). 2016. PMID: 26710928
Pseudo-Roberts Syndrome: An Entity or Not?
Salari B, Dehner LP. Salari B, et al. Fetal Pediatr Pathol. 2022 Jun;41(3):396-402. doi: 10.1080/15513815.2020.1827320. Epub 2020 Oct 7. Fetal Pediatr Pathol. 2022. PMID: 33026893
A child with Roberts syndrome.
Abbas R, Waqar S, Ahmad TM, Irfan Waheed KA, Sultan T, Qureshi AU. Abbas R, et al. J Coll Physicians Surg Pak. 2011 Jul;21(7):431-3. J Coll Physicians Surg Pak. 2011. PMID: 21777535
Phenotypic variability in 49 cases of ESCO2 mutations, including novel missense and codon deletion in the acetyltransferase domain, correlates with ESCO2 expression and establishes the clinical criteria for Roberts syndrome.
Vega H, Trainer AH, Gordillo M, Crosier M, Kayserili H, Skovby F, Uzielli ML, Schnur RE, Manouvrier S, Blair E, Hurst JA, Forzano F, Meins M, Simola KO, Raas-Rothschild A, Hennekam RC, Jabs EW. Vega H, et al. J Med Genet. 2010 Jan;47(1):30-7. doi: 10.1136/jmg.2009.068395. Epub 2009 Jul 1. J Med Genet. 2010. PMID: 19574259
205 results