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

Year Number of Results
1990 1
1994 2
1998 1
1999 3
2000 1
2001 2
2002 2
2003 3
2004 2
2005 1
2006 3
2007 3
2008 5
2009 7
2010 3
2011 6
2012 6
2013 2
2014 1
2015 1
2016 2
2023 0
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48 results
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Page 1
Isochromosome-formation in chromosome 9.
Miller K, Arslan-Kirchner M. Miller K, et al. Among authors: arslan kirchner m. Ann Genet. 1994;37(2):78-81. Ann Genet. 1994. PMID: 7985983 Review.
Patient with trisomy 6 mosaicism.
Miller KR, Mühlhaus K, Herbst RA, Bohnhorst B, Böhmer S, Arslan-Kirchner M. Miller KR, et al. Among authors: arslan kirchner m. Am J Med Genet. 2001 Apr 22;100(2):103-5. Am J Med Genet. 2001. PMID: 11298369
The new Ghent criteria for Marfan syndrome: what do they change?
Faivre L, Collod-Beroud G, Adès L, Arbustini E, Child A, Callewaert BL, Loeys B, Binquet C, Gautier E, Mayer K, Arslan-Kirchner M, Grasso M, Beroud C, Hamroun D, Bonithon-Kopp C, Plauchu H, Robinson PN, De Backer J, Coucke P, Francke U, Bouchot O, Wolf JE, Stheneur C, Hanna N, Detaint D, De Paepe A, Boileau C, Jondeau G. Faivre L, et al. Among authors: arslan kirchner m. Clin Genet. 2012 May;81(5):433-42. doi: 10.1111/j.1399-0004.2011.01703.x. Epub 2011 Jun 2. Clin Genet. 2012. PMID: 21564093 Free article.
Clinical utility gene card for: Hereditary thoracic aortic aneurysm and dissection including next-generation sequencing-based approaches.
Arslan-Kirchner M, Arbustini E, Boileau C, Charron P, Child AH, Collod-Beroud G, De Backer J, De Paepe A, Dierking A, Faivre L, Hoffjan S, Jondeau G, Keyser B, Loeys B, Mayer K, Robinson PN, Schmidtke J. Arslan-Kirchner M, et al. Eur J Hum Genet. 2016 Jan;24(1):e1-5. doi: 10.1038/ejhg.2015.225. Epub 2015 Oct 28. Eur J Hum Genet. 2016. PMID: 26508578 Free PMC article. No abstract available.
Analysis of phenotype and genotype information for the diagnosis of Marfan syndrome.
Sheikhzadeh S, Kade C, Keyser B, Stuhrmann M, Arslan-Kirchner M, Rybczynski M, Bernhardt AM, Habermann CR, Hillebrand M, Mir T, Robinson PN, Berger J, Detter C, Blankenberg S, Schmidtke J, von Kodolitsch Y. Sheikhzadeh S, et al. Among authors: arslan kirchner m. Clin Genet. 2012 Sep;82(3):240-7. doi: 10.1111/j.1399-0004.2011.01771.x. Epub 2011 Oct 5. Clin Genet. 2012. PMID: 21883168
Prognosis factors in probands with an FBN1 mutation diagnosed before the age of 1 year.
Stheneur C, Faivre L, Collod-Béroud G, Gautier E, Binquet C, Bonithon-Kopp C, Claustres M, Child AH, Arbustini E, Adès LC, Francke U, Mayer K, Arslan-Kirchner M, De Paepe A, Chevallier B, Bonnet D, Jondeau G, Boileau C. Stheneur C, et al. Among authors: arslan kirchner m. Pediatr Res. 2011 Mar;69(3):265-70. doi: 10.1203/PDR.0b013e3182097219. Pediatr Res. 2011. PMID: 21135753 Free article.
Cardiovascular manifestations in men and women carrying a FBN1 mutation.
Détaint D, Faivre L, Collod-Beroud G, Child AH, Loeys BL, Binquet C, Gautier E, Arbustini E, Mayer K, Arslan-Kirchner M, Stheneur C, Halliday D, Beroud C, Bonithon-Kopp C, Claustres M, Plauchu H, Robinson PN, Kiotsekoglou A, De Backer J, Adès L, Francke U, De Paepe A, Boileau C, Jondeau G. Détaint D, et al. Among authors: arslan kirchner m. Eur Heart J. 2010 Sep;31(18):2223-9. doi: 10.1093/eurheartj/ehq258. Epub 2010 Aug 13. Eur Heart J. 2010. PMID: 20709720 Free article.
48 results