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

Year Number of Results
1995 2
1998 2
2000 1
2004 2
2005 2
2008 1
2011 1
2018 2
2021 1
2024 0

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PubMed (cited) for id: 605022

14 results

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Page 1
Dominant monoallelic variant in the PAK2 gene causes Knobloch syndrome type 2.
Antonarakis SE, Holoubek A, Rapti M, Rademaker J, Meylan J, Iwaszkiewicz J, Zoete V, Wilson C, Taylor J, Ansar M, Borel C, Menzel O, Kuželová K, Santoni FA. Antonarakis SE, et al. Hum Mol Genet. 2021 Dec 17;31(1):1-9. doi: 10.1093/hmg/ddab026. Hum Mol Genet. 2021. PMID: 33693784
UnPAKing the class differences among p21-activated kinases.
Eswaran J, Soundararajan M, Kumar R, Knapp S. Eswaran J, et al. Trends Biochem Sci. 2008 Aug;33(8):394-403. doi: 10.1016/j.tibs.2008.06.002. Epub 2008 Jul 17. Trends Biochem Sci. 2008. PMID: 18639460 Review.
3q29 microdeletion syndrome: clinical and molecular characterization of a new syndrome.
Willatt L, Cox J, Barber J, Cabanas ED, Collins A, Donnai D, FitzPatrick DR, Maher E, Martin H, Parnau J, Pindar L, Ramsay J, Shaw-Smith C, Sistermans EA, Tettenborn M, Trump D, de Vries BB, Walker K, Raymond FL. Willatt L, et al. Am J Hum Genet. 2005 Jul;77(1):154-60. doi: 10.1086/431653. Epub 2005 May 25. Am J Hum Genet. 2005. PMID: 15918153 Free PMC article.
14 results