Transient t(Y;1)(q12;q21) in a patient with Fanconi anemia and myelodysplastic syndrome
β Scribed by P.W. Thompson; G.R. Standen; A.D. Geddes
- Book ID
- 119105141
- Publisher
- Elsevier Science
- Year
- 1991
- Tongue
- English
- Weight
- 71 KB
- Volume
- 52
- Category
- Article
- ISSN
- 0165-4608
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A 49-year-old woman patient with atypical myelodysplastic syndrome (MDS) showing a der(3)t(3;12)(q21;p13), and der(12)t(3; 12)(q21;p13)inv(3)(q21q26) as an acquired chromosomal abnormality in the bone marrow is described. The chromosomal breakpoints of the presented complex aberration with combinati
## Abstract Several cases of mos 46,X,der(Y)t(Y;1)(q12;q21)/46,XY with multiple anomalies have been reported. I report on an additional case of a male fetus with a mosaic male karyotype mos 46,X,der(Y)t(Y;1)(q12;q21)[31]/46,XY[21] and multiple anomalies that included βteardropββshaped head with a t