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Phenotypically concordant and discordant monozygotic twins display different DNA copy-number-variation profiles.
Am J Hum Genet. 2008 Mar;82(3):763-71. doi: 10.1016/j.ajhg.2007.12.011. Epub 2008 Feb 14.
Am J Hum Genet. 2008.
PMID: 18304490
Free PMC article.
Profiling of copy number variations (CNVs) in healthy individuals from three ethnic groups using a human genome 32 K BAC-clone-based array.
Díaz de Ståhl T, Sandgren J, Piotrowski A, Nord H, Andersson R, Menzel U, Bogdan A, Thuresson AC, Poplawski A, von Tell D, Hansson CM, Elshafie AI, Elghazali G, Imreh S, Nordenskjöld M, Upadhyaya M, Komorowski J, Bruder CE, Dumanski JP.
Díaz de Ståhl T, et al. Among authors: von tell d.
Hum Mutat. 2008 Mar;29(3):398-408. doi: 10.1002/humu.20659.
Hum Mutat. 2008.
PMID: 18058796
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Somatic mosaicism for copy number variation in differentiated human tissues.
Piotrowski A, Bruder CE, Andersson R, Diaz de Ståhl T, Menzel U, Sandgren J, Poplawski A, von Tell D, Crasto C, Bogdan A, Bartoszewski R, Bebok Z, Krzyzanowski M, Jankowski Z, Partridge EC, Komorowski J, Dumanski JP.
Piotrowski A, et al. Among authors: von tell d.
Hum Mutat. 2008 Sep;29(9):1118-24. doi: 10.1002/humu.20815.
Hum Mutat. 2008.
PMID: 18570184
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Refined mapping of the Welander distal myopathy region on chromosome 2p13 positions the new candidate region telomeric of the DYSF locus.
von Tell D, Bruder CE, Anderson LV, Anvret M, Ahlberg G.
von Tell D, et al.
Neurogenetics. 2003 Aug;4(4):173-7. doi: 10.1007/s10048-003-0154-z. Epub 2003 Jun 27.
Neurogenetics. 2003.
PMID: 12836053
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Genetic linkage of Welander distal myopathy to chromosome 2p13.
Ahlberg G, von Tell D, Borg K, Edström L, Anvret M.
Ahlberg G, et al. Among authors: von tell d.
Ann Neurol. 1999 Sep;46(3):399-404. doi: 10.1002/1531-8249(199909)46:3<399::aid-ana16>3.0.co;2-q.
Ann Neurol. 1999.
PMID: 10482271
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Welander distal myopathy outside the Swedish population: phenotype and genotype.
von Tell D, Somer H, Udd B, Edström L, Borg K, Ahlberg G.
von Tell D, et al.
Neuromuscul Disord. 2002 Aug;12(6):544-7. doi: 10.1016/s0960-8966(01)00338-8.
Neuromuscul Disord. 2002.
PMID: 12117477
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A heterozygous frameshift mutation in the endothelin-3 (EDN-3) gene in isolated Hirschsprung's disease.
Svensson PJ, Von Tell D, Molander ML, Anvret M, Nordenskjöld A.
Svensson PJ, et al. Among authors: von tell d.
Pediatr Res. 1999 May;45(5 Pt 1):714-7. doi: 10.1203/00006450-199905010-00018.
Pediatr Res. 1999.
PMID: 10231870
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Pericytes and vascular stability.
von Tell D, Armulik A, Betsholtz C.
von Tell D, et al.
Exp Cell Res. 2006 Mar 10;312(5):623-9. doi: 10.1016/j.yexcr.2005.10.019. Epub 2005 Nov 21.
Exp Cell Res. 2006.
PMID: 16303125
Review.
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