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Further characterization of the 9q31 microdeletion phenotype; delineation of a common region of overlap containing ZNF462.
Mol Genet Genomic Med. 2023 Mar;11(3):e2116. doi: 10.1002/mgg3.2116. Epub 2022 Dec 3.
Mol Genet Genomic Med. 2023.
PMID: 36461789
Free PMC article.
Constitutional chromothripsis involving chromosome 19 in a child with subtle dysmorphic features.
Wang JC, Fisker T, Sahoo T.
Wang JC, et al. Among authors: fisker t.
Am J Med Genet A. 2015 Apr;167A(4):910-3. doi: 10.1002/ajmg.a.36962. Epub 2015 Mar 3.
Am J Med Genet A. 2015.
PMID: 25736334
No abstract available.
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Chromosome 6 between-arm intrachromosomal insertion with intrasegmental double inversion: a four-break model.
Wang JC, Dang L, Fisker T.
Wang JC, et al. Among authors: fisker t.
Am J Med Genet A. 2010 Jan;152A(1):209-11. doi: 10.1002/ajmg.a.33161.
Am J Med Genet A. 2010.
PMID: 20034066
No abstract available.
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4.3-Mb triplication of 4q32.1-q32.2: report of a family through two generations.
Wang JC, Fisker T, Dang L, Teshima I, Nowaczyk MJ.
Wang JC, et al. Among authors: fisker t.
Am J Med Genet A. 2009 Oct;149A(10):2274-9. doi: 10.1002/ajmg.a.33020.
Am J Med Genet A. 2009.
PMID: 19764020
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Experiences of surviving spouse of terminally ill spouse: a phenomenological study of an altruistic perspective.
Fisker T, Strandmark M.
Fisker T, et al.
Scand J Caring Sci. 2007 Jun;21(2):274-81. doi: 10.1111/j.1471-6712.2007.00466.x.
Scand J Caring Sci. 2007.
PMID: 17559447
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