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

Year Number of Results
2003 1
2005 3
2006 3
2008 4
2009 3
2016 1
2017 1
2022 0
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13 results
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Page 1
Identification of new mutations in the TBX5 gene in patients with Holt-Oram syndrome.
Heinritz W, Moschik A, Kujat A, Spranger S, Heilbronner H, Demuth S, Bier A, Tihanyi M, Mundlos S, Gruenauer-Kloevekorn C, Froster UG. Heinritz W, et al. Among authors: gruenauer kloevekorn c. Heart. 2005 Mar;91(3):383-4. doi: 10.1136/hrt.2004.036855. Heart. 2005. PMID: 15710732 Free PMC article. No abstract available.
TGFBI (BIGH3) gene mutations in German families: two novel mutations associated with unique clinical and histopathological findings.
Gruenauer-Kloevekorn C, Clausen I, Weidle E, Wolter-Roessler M, Tost F, Völcker HE, Schulze DP, Heinritz W, Reinhard T, Froster U, Duncker G, Schorderet D, Auw-Haedrich C. Gruenauer-Kloevekorn C, et al. Br J Ophthalmol. 2009 Jul;93(7):932-7. doi: 10.1136/bjo.2008.142927. Epub 2008 Nov 10. Br J Ophthalmol. 2009. PMID: 19001012
13 results