Discover open access scientific publications

Search, annotate, share and cite publications

Publications by S S Kadkol

Molecular Identification of CBFβ-MYH11 Fusion Transcripts in an AML M4Eo Patient in the Absence of Inv16 or Other Abnormality by Cytogenetic and FISH Analyses – A Rare Occurrence

Leukemia

English

Related publications

Acute Myeloblastic Leukemia (AML) With Inv (16)(p13;q22) and the Rare I Type CBFβ-MYH11 Transcript: Report of Two New Cases

English

Identification of Candidate Neoantigens Produced by Fusion Transcripts in Human Osteosarcomas

Scientific Reports

Multidisciplinary

2019

English

Acquisition of the Ph Chromosome and BCR-ABL Fusion Product in AML-M2 and T(8;21) Leukemia: Cytogenetic and FISH Evidence for a Late Event

English

Cytogenetic, Molecular and FISH Analysis of an Isodicentric Chromosome 21 Idic(21)(q22.3) in a Mildly-Affected Patient With Down Syndrome

International Journal of Human Genetics

Genetics

2007

English

Therapy-Related Myelodysplastic Syndrome With Inv(16)(p13q22) and I Type CBFβ/MYH11 After Autologous Transplantation: Undetectable Fusion Transcript in Pretransplant Progenitor Cells

English

Simultaneous Occurrence of BCR-Abl and Inv16 in a Case of M1 Acute Myeloid Leukemia

English

Cryptic Insertion and Translocation or Nondividing Leukemic Cells Disclosed by FISH Analysis in Infant Acute Leukemia With Discrepant Molecular and Cytogenetic Findings

English

TopHat-Fusion: An Algorithm for Discovery of Novel Fusion Transcripts

Genome Biology

2011

English

An Accumulation of Cytogenetic and Molecular Genetic Events Characterizes the Progression From MDS to Secondary AML: An Analysis of 38 Paired Samples Analyzed by Cytogenetics, Molecular Mutation Analysis and SNP Microarray Profiling

English

Amanote Research

Discover open access scientific publications

Search, annotate, share and cite publications

Publications by S S Kadkol

Molecular Identification of CBFβ-MYH11 Fusion Transcripts in an AML M4Eo Patient in the Absence of Inv16 or Other Abnormality by Cytogenetic and FISH Analyses – A Rare Occurrence

Related publications

Acute Myeloblastic Leukemia (AML) With Inv (16)(p13;q22) and the Rare I Type CBFβ-MYH11 Transcript: Report of Two New Cases

Identification of Candidate Neoantigens Produced by Fusion Transcripts in Human Osteosarcomas

Acquisition of the Ph Chromosome and BCR-ABL Fusion Product in AML-M2 and T(8;21) Leukemia: Cytogenetic and FISH Evidence for a Late Event

Cytogenetic, Molecular and FISH Analysis of an Isodicentric Chromosome 21 Idic(21)(q22.3) in a Mildly-Affected Patient With Down Syndrome

Therapy-Related Myelodysplastic Syndrome With Inv(16)(p13q22) and I Type CBFβ/MYH11 After Autologous Transplantation: Undetectable Fusion Transcript in Pretransplant Progenitor Cells

Simultaneous Occurrence of BCR-Abl and Inv16 in a Case of M1 Acute Myeloid Leukemia

Cryptic Insertion and Translocation or Nondividing Leukemic Cells Disclosed by FISH Analysis in Infant Acute Leukemia With Discrepant Molecular and Cytogenetic Findings

TopHat-Fusion: An Algorithm for Discovery of Novel Fusion Transcripts

An Accumulation of Cytogenetic and Molecular Genetic Events Characterizes the Progression From MDS to Secondary AML: An Analysis of 38 Paired Samples Analyzed by Cytogenetics, Molecular Mutation Analysis and SNP Microarray Profiling