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De novo AML with trilineage myelodysplasia and a novel t(11;12)(p15;q13)

โœ Scribed by K.F Wong; Y.L Kwong; C.C So


Book ID
114136263
Publisher
Elsevier Science
Year
1998
Tongue
English
Weight
190 KB
Volume
100
Category
Article
ISSN
0165-4608

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Familial translocation t(Y;15)(q12;p11)
โœ Eliez, Stephan; Morris, Michael A.; Dahoun-Hadorn, Sophie; DeLozier-Blanchet, C. ๐Ÿ“‚ Article ๐Ÿ“… 1997 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 351 KB ๐Ÿ‘ 1 views

We describe a 17-year-old girl with mild Prader-Willi syndrome (PWS) due to 15q11-q13 deletion. The deletion occurred on a paternal chromosome 15 already involved in a translocation, t(Y;15)(q12;p11), the latter being present in five other, phenotypically normal individuals in three generations. Thi