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

Year Number of Results
1991 1
1992 2
1993 3
1994 3
1995 1
1996 2
1997 2
1998 3
1999 4
2000 1
2001 1
2002 1
2003 4
2004 3
2005 4
2006 3
2007 1
2008 6
2009 1
2010 2
2011 1
2012 4
2013 1
2014 3
2015 1
2018 1
2019 2
2020 3
2024 0

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62 results

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Page 1
Functional basic reading skills in Williams syndrome.
Brawn G, Kohnen S, Tassabehji M, Porter M. Brawn G, et al. Among authors: tassabehji m. Dev Neuropsychol. 2018;43(5):454-477. doi: 10.1080/87565641.2018.1455838. Epub 2018 Mar 30. Dev Neuropsychol. 2018. PMID: 29601225
LIM-kinase deleted in Williams syndrome.
Tassabehji M, Metcalfe K, Fergusson WD, Carette MJ, Dore JK, Donnai D, Read AP, Pröschel C, Gutowski NJ, Mao X, Sheer D. Tassabehji M, et al. Nat Genet. 1996 Jul;13(3):272-3. doi: 10.1038/ng0796-272. Nat Genet. 1996. PMID: 8673124 No abstract available.
The mutational spectrum in Waardenburg syndrome.
Tassabehji M, Newton VE, Liu XZ, Brady A, Donnai D, Krajewska-Walasek M, Murday V, Norman A, Obersztyn E, Reardon W, et al. Tassabehji M, et al. Hum Mol Genet. 1995 Nov;4(11):2131-7. doi: 10.1093/hmg/4.11.2131. Hum Mol Genet. 1995. PMID: 8589691
GORAB scaffolds COPI at the trans-Golgi for efficient enzyme recycling and correct protein glycosylation.
Witkos TM, Chan WL, Joensuu M, Rhiel M, Pallister E, Thomas-Oates J, Mould AP, Mironov AA, Biot C, Guerardel Y, Morelle W, Ungar D, Wieland FT, Jokitalo E, Tassabehji M, Kornak U, Lowe M. Witkos TM, et al. Among authors: tassabehji m. Nat Commun. 2019 Jan 10;10(1):127. doi: 10.1038/s41467-018-08044-6. Nat Commun. 2019. PMID: 30631079 Free PMC article.
62 results