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Table representation of search results timeline featuring number of search results per year.
Year
Number of Results
1976
1
1977
3
1978
4
1979
6
1980
7
1981
7
1982
6
1983
14
1984
3
1985
8
1986
5
1987
6
1988
8
1989
8
1990
8
1991
11
1992
5
1993
4
1994
8
1995
5
1996
2
1997
7
1998
3
1999
1
2000
5
2001
5
2002
7
2003
5
2004
13
2005
4
2006
5
2007
12
2008
9
2009
9
2010
8
2011
8
2012
7
2013
15
2014
18
2015
15
2016
7
2017
11
2018
11
2019
12
2020
18
2021
9
2022
13
2023
7
2024
3
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Page 1
Teschler-Nicola/Killian syndrome.
Pagon RA.
Pagon RA.
J Clin Dysmorphol. 1983 Fall;1(3):18-9.
J Clin Dysmorphol. 1983.
PMID: 6584556
No abstract available.
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Muscle-eye-brain disease (MEB).
Santavuori P, Somer H, Sainio K, Rapola J, Kruus S, Nikitin T, Ketonen L, Leisti J.
Santavuori P, et al.
Brain Dev. 1989;11(3):147-53. doi: 10.1016/s0387-7604(89)80088-9.
Brain Dev. 1989.
PMID: 2751061
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Pregnancy in 3M syndrome.
Cusimano MC, Chitayat D, Injeyan M, Geary M.
Cusimano MC, et al.
J Obstet Gynaecol. 2018 Apr;38(3):421-422. doi: 10.1080/01443615.2017.1360849. Epub 2017 Oct 19.
J Obstet Gynaecol. 2018.
PMID: 29046114
No abstract available.
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HECW2-related disorder in four Japanese patients.
Yanagishita T, Hirade T, Shimojima Yamamoto K, Funatsuka M, Miyamoto Y, Maeda M, Yanagi K, Kaname T, Nagata S, Nagata M, Ishihara Y, Miyashita Y, Asano Y, Sakata Y, Kosaki K, Yamamoto T.
Yanagishita T, et al.
Am J Med Genet A. 2021 Oct;185(10):2895-2902. doi: 10.1002/ajmg.a.62363. Epub 2021 May 28.
Am J Med Genet A. 2021.
PMID: 34047014
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Congenital Hypotonia in Toddlerhood.
Steiner N, Torres A, Reddy A, Augustyn M.
Steiner N, et al.
J Dev Behav Pediatr. 2017 Sep;38(7):556-557. doi: 10.1097/DBP.0000000000000497.
J Dev Behav Pediatr. 2017.
PMID: 28816914
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Movement disorders in MCT8 deficiency/Allan-Herndon-Dudley Syndrome.
Masnada S, Sarret C, Antonello CE, Fadilah A, Krude H, Mura E, Mordekar S, Nicita F, Olivotto S, Orcesi S, Porta F, Remerand G, Siri B, Wilpert NM, Amir-Yazdani P, Bertini E, Schuelke M, Bernard G, Boespflug-Tanguy O, Tonduti D.
Masnada S, et al.
Mol Genet Metab. 2022 Jan;135(1):109-113. doi: 10.1016/j.ymgme.2021.12.003. Epub 2021 Dec 16.
Mol Genet Metab. 2022.
PMID: 34969638
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