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Deletion of 14.7 Mb 2q32.3q33.3 with a marfanoid phenotype and hypothyroidism.
Am J Med Genet A. 2013 Sep;161A(9):2347-51. doi: 10.1002/ajmg.a.36076. Epub 2013 Aug 5.
Am J Med Genet A. 2013.
PMID: 23918240
A familial deletion of 16q21 characterized by an SNP array and associated with a normal phenotype.
Kowalczyk M, Tomaszewska A, Podbiol-Palenta A, Remiszewska B, Galjaard RJ, Zajaczek S, Srebniak MI.
Kowalczyk M, et al. Among authors: podbiol palenta a.
Am J Med Genet A. 2013 Jun;161A(6):1501-4. doi: 10.1002/ajmg.a.35912. Epub 2013 Apr 30.
Am J Med Genet A. 2013.
PMID: 23633153
No abstract available.
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The first de novo non-mosaic 14q11.2q13.1 tetrasomy of paternal origin.
Tomaszewska A, Behrendt J, Boter M, Wawrzkiewicz-Witkowska A, Bos MJ, Podbiol-Palenta A, Godula-Stuglik U, Galjaard RJ, Srebniak MI.
Tomaszewska A, et al. Among authors: podbiol palenta a.
Am J Med Genet A. 2016 May;170A(5):1283-7. doi: 10.1002/ajmg.a.37565. Epub 2016 Jan 20.
Am J Med Genet A. 2016.
PMID: 26789739
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Another rare case of a child with de novo terminal 9p deletion and co-existing interstitial 9p duplication: clinical findings and molecular cytogenetic study by array-CGH.
Kowalczyk M, Tomaszewska A, Podbioł-Palenta A, Constantinou M, Wawrzkiewicz-Witkowska A, Kowalski J, Kałużewski B, Zajączek S, Srebniak MI.
Kowalczyk M, et al. Among authors: podbiol palenta a.
Cytogenet Genome Res. 2013;139(1):9-16. doi: 10.1159/000342165. Epub 2012 Sep 5.
Cytogenet Genome Res. 2013.
PMID: 22965227
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