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

Year Number of Results
1961 2
1965 1
1989 1
1991 1
1992 1
1993 1
2000 2
2001 3
2002 1
2003 1
2005 1
2007 1
2008 1
2009 1
2010 1
2011 4
2012 3
2014 2
2015 4
2016 1
2017 1
2018 1
2019 5
2020 1
2021 3
2023 1
2024 1

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40 results

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Page 1
ClinGen--the Clinical Genome Resource.
Rehm HL, Berg JS, Brooks LD, Bustamante CD, Evans JP, Landrum MJ, Ledbetter DH, Maglott DR, Martin CL, Nussbaum RL, Plon SE, Ramos EM, Sherry ST, Watson MS; ClinGen. Rehm HL, et al. N Engl J Med. 2015 Jun 4;372(23):2235-42. doi: 10.1056/NEJMsr1406261. Epub 2015 May 27. N Engl J Med. 2015. PMID: 26014595 Free PMC article.
The Stickler syndrome: genotype/phenotype correlation in 10 families with Stickler syndrome resulting from seven mutations in the type II collagen gene locus COL2A1.
Liberfarb RM, Levy HP, Rose PS, Wilkin DJ, Davis J, Balog JZ, Griffith AJ, Szymko-Bennett YM, Johnston JJ, Francomano CA, Tsilou E, Rubin BI. Liberfarb RM, et al. Among authors: levy hp. Genet Med. 2003 Jan-Feb;5(1):21-7. doi: 10.1097/00125817-200301000-00004. Genet Med. 2003. PMID: 12544472 Free article. Review.
Natural history of aging in Cornelia de Lange syndrome.
Kline AD, Grados M, Sponseller P, Levy HP, Blagowidow N, Schoedel C, Rampolla J, Clemens DK, Krantz I, Kimball A, Pichard C, Tuchman D. Kline AD, et al. Among authors: levy hp. Am J Med Genet C Semin Med Genet. 2007 Aug 15;145C(3):248-60. doi: 10.1002/ajmg.c.30137. Am J Med Genet C Semin Med Genet. 2007. PMID: 17640042 Free PMC article. Review.
Chromosome instability syndromes.
Cohen MM, Levy HP. Cohen MM, et al. Among authors: levy hp. Adv Hum Genet. 1989;18:43-149, 365-71. doi: 10.1007/978-1-4613-0785-3_2. Adv Hum Genet. 1989. PMID: 2658496 Review. No abstract available.
The hip in Stickler syndrome.
Rose PS, Ahn NU, Levy HP, Magid D, Davis J, Liberfarb RM, Sponseller PD, Francomano CA. Rose PS, et al. Among authors: levy hp. J Pediatr Orthop. 2001 Sep-Oct;21(5):657-63. J Pediatr Orthop. 2001. PMID: 11521037
Application of a framework to guide genetic testing communication across clinical indications.
Hallquist MLG, Tricou EP, Ormond KE, Savatt JM, Coughlin CR 2nd, Faucett WA, Hercher L, Levy HP, O'Daniel JM, Peay HL, Stosic M, Smith M, Uhlmann WR, Wand H, Wain KE, Buchanan AH. Hallquist MLG, et al. Among authors: levy hp. Genome Med. 2021 Apr 29;13(1):71. doi: 10.1186/s13073-021-00887-x. Genome Med. 2021. PMID: 33926532 Free PMC article.
40 results