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Genetic aspects of shell teeth: report of case.
Kamen S, Goodman D, Heimler A. Kamen S, et al. Among authors: heimler a. ASDC J Dent Child. 1980 May-Jun;47(3):187-9. ASDC J Dent Child. 1980. PMID: 6929799 No abstract available.
Heimler Syndrome Is Caused by Hypomorphic Mutations in the Peroxisome-Biogenesis Genes PEX1 and PEX6.
Ratbi I, Falkenberg KD, Sommen M, Al-Sheqaih N, Guaoua S, Vandeweyer G, Urquhart JE, Chandler KE, Williams SG, Roberts NA, El Alloussi M, Black GC, Ferdinandusse S, Ramdi H, Heimler A, Fryer A, Lynch SA, Cooper N, Ong KR, Smith CE, Inglehearn CF, Mighell AJ, Elcock C, Poulter JA, Tischkowitz M, Davies SJ, Sefiani A, Mironov AA, Newman WG, Waterham HR, Van Camp G. Ratbi I, et al. Among authors: heimler a. Am J Hum Genet. 2015 Oct 1;97(4):535-45. doi: 10.1016/j.ajhg.2015.08.011. Epub 2015 Sep 17. Am J Hum Genet. 2015. PMID: 26387595 Free PMC article.
Letters to the editor.
Heimler A, Hodge SE. Heimler A, et al. J Genet Couns. 1996 Jun;5(2):93-9. doi: 10.1007/BF01408536. J Genet Couns. 1996. PMID: 24234595 No abstract available.
Testing for HD in twins.
Reich E, Zanko A, Heimler A. Reich E, et al. Among authors: heimler a. J Genet Couns. 1996 Mar;5(1):47-51. doi: 10.1007/BF01408667. J Genet Couns. 1996. PMID: 11657408 No abstract available.
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