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

Year Number of Results
1990 2
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1992 4
1994 1
1996 1
2000 1
2001 1
2002 1
2004 2
2005 1
2008 1
2009 1
2012 4
2013 3
2014 2
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2019 1
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2024 0

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31 results

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Page 1
Elucidating the diagnostic odyssey of 22q11.2 deletion syndrome.
Palmer LD, Butcher NJ, Boot E, Hodgkinson KA, Heung T, Chow EWC, Guna A, Crowley TB, Zackai E, McDonald-McGinn DM, Bassett AS. Palmer LD, et al. Among authors: hodgkinson ka. Am J Med Genet A. 2018 Apr;176(4):936-944. doi: 10.1002/ajmg.a.38645. Am J Med Genet A. 2018. PMID: 29575622 Free PMC article.
A pathogenic deletion in Forkhead Box L1 (FOXL1) identifies the first otosclerosis (OTSC) gene.
Abdelfatah N, Mostafa AA, French CR, Doucette LP, Penney C, Lucas MB, Griffin A, Booth V, Rowley C, Besaw JE, Tranebjærg L, Rendtorff ND, Hodgkinson KA, Little LA, Agrawal S, Parnes L, Batten T, Moore S, Hu P, Pater JA, Houston J, Galutira D, Benteau T, MacDonald C, French D, O'Rielly DD, Stanton SG, Young TL. Abdelfatah N, et al. Among authors: hodgkinson ka. Hum Genet. 2022 Apr;141(3-4):965-979. doi: 10.1007/s00439-021-02381-1. Epub 2021 Oct 11. Hum Genet. 2022. PMID: 34633540 Free PMC article.
All-cause mortality and survival in adults with 22q11.2 deletion syndrome.
Van L, Heung T, Graffi J, Ng E, Malecki S, Van Mil S, Boot E, Corral M, Chow EWC, Hodgkinson KA, Silversides C, Bassett AS. Van L, et al. Among authors: hodgkinson ka. Genet Med. 2019 Oct;21(10):2328-2335. doi: 10.1038/s41436-019-0509-y. Epub 2019 Apr 5. Genet Med. 2019. PMID: 30948858 Free PMC article.
Reproductive fitness in familial schizophrenia.
Bassett AS, Bury A, Hodgkinson KA, Honer WG. Bassett AS, et al. Among authors: hodgkinson ka. Schizophr Res. 1996 Sep 18;21(3):151-60. doi: 10.1016/0920-9964(96)00018-7. Schizophr Res. 1996. PMID: 8885043 Free PMC article.
Bundle Branch Re-Entrant Ventricular Tachycardia: Novel Genetic Mechanisms in a Life-Threatening Arrhythmia.
Roberts JD, Gollob MH, Young C, Connors SP, Gray C, Wilton SB, Green MS, Zhu DW, Hodgkinson KA, Poon A, Li Q, Orr N, Tang AS, Klein GJ, Wojciak J, Campagna J, Olgin JE, Badhwar N, Vedantham V, Marcus GM, Kwok PY, Deo RC, Scheinman MM. Roberts JD, et al. Among authors: hodgkinson ka. JACC Clin Electrophysiol. 2017 Mar;3(3):276-288. doi: 10.1016/j.jacep.2016.09.019. Epub 2016 Dec 21. JACC Clin Electrophysiol. 2017. PMID: 29759522 Free article.
Premature death in adults with 22q11.2 deletion syndrome.
Bassett AS, Chow EW, Husted J, Hodgkinson KA, Oechslin E, Harris L, Silversides C. Bassett AS, et al. Among authors: hodgkinson ka. J Med Genet. 2009 May;46(5):324-30. doi: 10.1136/jmg.2008.063800. Epub 2009 Feb 25. J Med Genet. 2009. PMID: 19246480 Free PMC article.
31 results