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Results by year

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

Year Number of Results
1974 1
1988 1
1994 1
1995 1
1998 1
1999 2
2001 3
2002 1
2003 1
2005 1
2006 4
2007 1
2008 2
2009 8
2011 2
2012 2
2013 3
2014 1
2015 3
2016 1
2017 2
2018 4
2019 1
2024 0

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PubMed (Bookshelf cited) for id: 315656

46 results

Results by year

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Page 1
Deletions and loss-of-function variants in TP63 associated with orofacial clefting.
Khandelwal KD, van den Boogaard MH, Mehrem SL, Gebel J, Fagerberg C, van Beusekom E, van Binsbergen E, Topaloglu O, Steehouwer M, Gilissen C, Ishorst N, van Rooij IALM, Roeleveld N, Christensen K, Schoenaers J, Bergé S, Murray JC, Hens G, Devriendt K, Ludwig KU, Mangold E, Hoischen A, Zhou H, Dötsch V, Carels CEL, van Bokhoven H. Khandelwal KD, et al. Eur J Hum Genet. 2019 Jul;27(7):1101-1112. doi: 10.1038/s41431-019-0370-0. Epub 2019 Mar 8. Eur J Hum Genet. 2019. PMID: 30850703 Free PMC article. Clinical Trial.
TAp63gamma is required for the late stages of myogenesis.
Cefalù S, Lena AM, Vojtesek B, Musarò A, Rossi A, Melino G, Candi E. Cefalù S, et al. Cell Cycle. 2015;14(6):894-901. doi: 10.4161/15384101.2014.988021. Cell Cycle. 2015. PMID: 25790093 Free PMC article.
Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.
Richards S, Aziz N, Bale S, Bick D, Das S, Gastier-Foster J, Grody WW, Hegde M, Lyon E, Spector E, Voelkerding K, Rehm HL; ACMG Laboratory Quality Assurance Committee. Richards S, et al. Genet Med. 2015 May;17(5):405-24. doi: 10.1038/gim.2015.30. Epub 2015 Mar 5. Genet Med. 2015. PMID: 25741868 Free PMC article.
46 results