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

Year Number of Results
1976 1
1978 4
1979 3
1980 1
1982 1
1984 2
1985 1
1987 4
1989 1
1990 2
1991 4
1992 1
1993 2
1994 2
1995 3
1996 2
1997 4
1998 1
1999 2
2000 1
2001 3
2002 2
2003 1
2004 1
2005 1
2006 2
2007 2
2008 3
2009 2
2010 3
2011 2
2012 7
2013 4
2014 7
2015 5
2016 6
2017 7
2018 4
2019 7
2020 3
2023 1
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Search Results

106 results
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Page 1
The duplication 17p13.3 phenotype: analysis of 21 families delineates developmental, behavioral and brain abnormalities, and rare variant phenotypes.
Curry CJ, Rosenfeld JA, Grant E, Gripp KW, Anderson C, Aylsworth AS, Saad TB, Chizhikov VV, Dybose G, Fagerberg C, Falco M, Fels C, Fichera M, Graakjaer J, Greco D, Hair J, Hopkins E, Huggins M, Ladda R, Li C, Moeschler J, Nowaczyk MJ, Ozmore JR, Reitano S, Romano C, Roos L, Schnur RE, Sell S, Suwannarat P, Svaneby D, Szybowska M, Tarnopolsky M, Tervo R, Tsai AC, Tucker M, Vallee S, Wheeler FC, Zand DJ, Barkovich AJ, Aradhya S, Shaffer LG, Dobyns WB. Curry CJ, et al. Among authors: aylsworth as. Am J Med Genet A. 2013 Aug;161A(8):1833-52. doi: 10.1002/ajmg.a.35996. Epub 2013 Jun 27. Am J Med Genet A. 2013. PMID: 23813913 Free PMC article.
Survival of children with trisomy 13 and trisomy 18: A multi-state population-based study.
Meyer RE, Liu G, Gilboa SM, Ethen MK, Aylsworth AS, Powell CM, Flood TJ, Mai CT, Wang Y, Canfield MA; National Birth Defects Prevention Network. Meyer RE, et al. Among authors: aylsworth as. Am J Med Genet A. 2016 Apr;170A(4):825-37. doi: 10.1002/ajmg.a.37495. Epub 2015 Dec 10. Am J Med Genet A. 2016. PMID: 26663415 Free PMC article.
Response to Hall et al.
Chong JX, Talbot JC, Teets EM, Previs S, Martin BL, Shively KM, Marvin CT, Aylsworth AS, Saadeh-Haddad R, Schatz UA, Inzana F, Ben-Omran T, Almusafri F, Al-Mulla M, Buckingham KJ, Harel T, Mor-Shaked H, Radhakrishnan P, Girisha KM, Nayak SS, Shukla A, Dieterich K, Faure J, Rendu J, Capri Y, Latypova X, Nickerson DA, Warshaw D, Janssen PM; University of Washington Center for Mendelian Genomics; Amacher SL, Bamshad MJ. Chong JX, et al. Among authors: aylsworth as. Am J Hum Genet. 2020 Dec 3;107(6):1188-1189. doi: 10.1016/j.ajhg.2020.11.006. Am J Hum Genet. 2020. PMID: 33275912 Free PMC article. No abstract available.
Camptodactyly and the 22q11.2 deletion syndrome.
Couser NL, Pande CK, Walsh JM, Tepperberg J, Aylsworth AS. Couser NL, et al. Among authors: aylsworth as. Am J Med Genet A. 2017 Feb;173(2):515-518. doi: 10.1002/ajmg.a.38029. Epub 2016 Oct 28. Am J Med Genet A. 2017. PMID: 27792854
106 results