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X monosomy and balanced Robertsonian translocation in a girl with Turner Syndrome
(Sociedade Brasileira de Genética, 2006-01-01)
We describe a case of X monosomy associated with a maternally inherited t(13;14) Robertsonian translocation in a girl with Turner syndrome. The girl's X chromosome was demonstrated to be maternally inherited, ruling out ...
X monosomy and balanced Robertsonian translocation in a girl with Turner Syndrome
(Sociedade Brasileira de Genética, 2006-01-01)
We describe a case of X monosomy associated with a maternally inherited t(13;14) Robertsonian translocation in a girl with Turner syndrome. The girl's X chromosome was demonstrated to be maternally inherited, ruling out ...
Clonal monosomy of chromosome 21 in a case of myelodysplastic syndrome
(Funpec-editora, 2011-01-01)
This study reports on a cytogenetic finding in a bone marrow examination of a 47-year-old male patient treated in the Hematology and Blood Transfusion Service of the Hospital de Base in Sao Jose do Rio Preto, Sao Paulo ...
Clonal monosomy of chromosome 21 in a case of myelodysplastic syndrome
(Funpec-editora, 2015)
X monosomy and balanced Robertsonian translocation in a girl with Turner Syndrome
(Sociedade Brasileira de Genética, 2014)
Clonal monosomy of chromosome 21 in a case of myelodysplastic syndrome
(Funpec-editora, 2015)
B lineage acute lymphoblastic leukemia transformation in a child with juvenile myelomonocytic leukemia, type 1 neurofibromatosis and monosomy of chromosome 7 - Possible implications in the leukemogenesis
(Elsevier B.V., 2003-04-01)
This report describes the case of an 8-month-old infant with a diagnosis of juvenile myelomonocytic leukemia (JMML) and type I neurofibromatosis that presented progression to B lineage acute lymphoid leukemia (ALL). The ...
B lineage acute lymphoblastic leukemia transformation in a child with juvenile myelomonocytic leukemia, type 1 neurofibromatosis and monosomy of chromosome 7 - Possible implications in the leukemogenesis
(Elsevier B.V., 2003-04-01)
This report describes the case of an 8-month-old infant with a diagnosis of juvenile myelomonocytic leukemia (JMML) and type I neurofibromatosis that presented progression to B lineage acute lymphoid leukemia (ALL). The ...