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Items: 3

1.
Characterization of a Rare Mosaicism in Autosomal Translocation of t(5;21) Using Conventional Cytogenetics and FISH Methods
Sadaf Omori Sarabi, Javad Karimzad Hagh, Claudia Behrend, Seyed Behrooz Mohseni, Mitra Ansari Dezfouli, Seyed Khalil Rashidi, Mir Davood Omrani
Iran Biomed J. 2020 Jan; 24(1): 60–63. Published online 2019 Jul 14. doi: 10.29252/ibj.24.1.60
PMCID:
PMC6900479
AbstractArticlePDF–917K
2.
Novel recurrent chromosomal aberrations detected in clonal plasma cells of light chain amyloidosis patients show potential adverse prognostic effect: first results from a genome-wide copy number array analysis
Martin Granzow, Ute Hegenbart, Katrin Hinderhofer, Dirk Hose, Anja Seckinger, Tilmann Bochtler, Kari Hemminki, Hartmut Goldschmidt, Stefan O. Schönland, Anna Jauch
Haematologica. 2017 Jul; 102(7): 1281–1290. Prepublished online 2017 Mar 24. doi: 10.3324/haematol.2016.160721
PMCID:
PMC5566044
AbstractArticlePDF–1016K
3.
Bilateral radial agenesis with absent thumbs, complex heart defect, short stature, and facial dysmorphism in a patient with pure distal microduplication of 5q35.2-5q35.3
Aleksander Jamsheer, Anna Sowińska, Dorota Simon, Małgorzata Jamsheer-Bratkowska, Tomasz Trzeciak, Anna Latos-Bieleńska
BMC Med Genet. 2013; 14: 13. Published online 2013 Jan 24. doi: 10.1186/1471-2350-14-13
PMCID:
PMC3576294
AbstractArticlePDF–966K

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