K. Rao

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Tyrosine kinase inhibitor therapy induces remission in a patient with refractory EBF1-PDGFRB-positive acute lymphoblastic leukemia.

C. Mullighan, K. Roberts, Kathleen W. Rao, 2013, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Prolonged subcutaneous administration of recombinant α2b interferon in patients with previously untreated Philadelphia chromosome-positive chronic-phase chronic myelogenous leukemia: Effect on remission duration and survival: Cancer and leukemia group B study 8583

C. Bloomfield, J. Testa, S. George, 1993 .

Group B study 8583 (see comments) effect on remission duration and survival: Cancer and Leukemia chromosome-positive chronic-phase chronic myelogenous leukemia: interferon in patients with previously untreated Philadelphia Prolonged subcutaneous administration of recombinant alpha 2b

S. George, A. Gottlieb, B. Peterson, 2011 .

Pretreatment cytogenetic abnormalities are predictive of induction success, cumulative incidence of relapse, and overall survival in adult patients with de novo acute myeloid leukemia: results from Cancer and Leukemia Group B (CALGB 8461).

C. Bloomfield, J. Byrd, R. Larson, 2002, Blood.

Pleomorphic liposarcoma: A cytologic study of five cases

L. Dodd, M. Bui, Kathleen W. Rao, 2015, Diagnostic Cytopathology.

Masked hypodiploidy: Hypodiploid acute lymphoblastic leukemia (ALL) mimicking hyperdiploid ALL in children: A report from the Children's Oncology Group.

M. Loh, M. Shago, S. Raimondi, 2019, Cancer genetics.

Cytogenetic and molecular characterization of A2BP1/FOX1 as a candidate gene for autism

Christa Lese Martin, D. Geschwind, E. Cook, 2007, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Structural Chromosome Rearrangements

Kathleen W. Rao, K. Kaiser-Rogers, K. Rao, 2005 .

The genetic architecture of Down syndrome phenotypes revealed by high-resolution analysis of human segmental trisomies

M. Gerstein, Fabian Grubert, L. Shaffer, 2009, Proceedings of the National Academy of Sciences.

Central review of cytogenetics is necessary for cooperative group correlative and clinical studies of adult acute leukemia: the Cancer and Leukemia Group B experience.

C. Bloomfield, M. Qumsiyeh, K. Mrózek, 2008, International journal of oncology.

Adult de novo acute myeloid leukemia with t(6;11)(q27;q23)

C. Bloomfield, R. Larson, K. Mrózek, 2004, Cancer.

Secondary cytogenetic changes in acute promyelocytic leukemia--prognostic importance in patients treated with chemotherapy alone and association with the intron 3 breakpoint of the PML gene: a Cancer and Leukemia Group B study.

C. Bloomfield, K. Mrózek, S. Bigner, 1997, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Clinical laboratory assays for HER-2/neu amplification and overexpression: quality assurance, standardization, and proficiency testing.

R. Nagle, G. Vance, A. Brothman, 2002, Archives of pathology & laboratory medicine.

Specific extra chromosomes occur in a modal number dependent pattern in pediatric acute lymphoblastic leukemia

S. Raimondi, James R. Anderson, W. Sanger, 2007, Genes, chromosomes & cancer.

MATERNAL UNIPARENTAL DISOMY OF CHROMOSOME 2 AND CONFINED PLACENTAL MOSAICISM FOR TRISOMY 2 IN A FETUS WITH INTRAUTERINE GROWTH RESTRICTION, HYPOSPADIAS, AND OLIGOHYDRAMNIOS

S. Langlois, A. Aylsworth, D. Smith, 1997, Prenatal diagnosis.

Section E9 of the American College of Medical Genetics technical standards and guidelines: Fluorescence in situ hybridization

H. Kearney, K. Tsuchiya, S. Olson, 2011, Genetics in Medicine.

Preliminary phenotypic map of chromosome 4p16 based on 4p deletions.

B. Korf, E. Ikonen, D. Driscoll, 1995, American journal of medical genetics.

New recurrent balanced translocations in acute myeloid leukemia and myelodysplastic syndromes: Cancer and leukemia group B 8461

C. Bloomfield, K. Mrózek, A. Carroll, 2013, Genes, chromosomes & cancer.

Section E 9 of the American College of Medical Genetics technical standards and guidelines : Fluorescence in situ hybridization

H. Kearney, K. Tsuchiya, S. Olson, 2011 .

patients with de novo acute myeloid leukemia : results from Cancer and success , cumulative incidence of relapse , and overall survival in adult Pretreatment cytogenetic abnormalities are predictive of induction

C. Bloomfield, J. Byrd, R. Larson, 2002 .

Two cases of acute myeloid leukemia with t(11;17) associated with varying morphology and immunophenotype: rearrangement of the MLL gene and a region proximal to the RARα gene

C. Dunphy, K. Kaiser-Rogers, L. Kang, 2005 .

Short communication Two cases of acute myeloid leukemia with t(11;17) associated with varying morphology and immunophenotype: rearrangement of the MLL gene and a region proximal to the RARa gene

C. Dunphy, K. Kaiser-Rogers, L. Kang, 2005 .

Adult patients with de novo acute myeloid leukemia and t(9; 11)(p22; q23) have a superior outcome to patients with other translocations involving band 11q23: a cancer and leukemia group B study.

C. Bloomfield, K. Mrózek, R. Mayer, 1997, Blood.

Guidance for fluorescence in situ hybridization testing in hematologic disorders.

P. N. Rao, A. Bagg, G. Dewald, 2007, The Journal of molecular diagnostics : JMD.

HER-2 fluorescence in situ hybridization: results from the survey program of the College of American Pathologists.

R. Tubbs, G. Dewald, J. Mascarello, 2006, Archives of pathology & laboratory medicine.

American College of Medical Genetics recommendations for the design and performance expectations for clinical genomic copy number microarrays intended for use in the postnatal setting for detection of constitutional abnormalities

S. South, A. Hamosh, H. Kearney, 2011, Genetics in Medicine.

Clinical applications of BCR-ABL molecular testing in acute leukemia.

M. Gulley, Kathleen W. Rao, A. Nashed, 2003, The Journal of molecular diagnostics : JMD.

Adult de novo acute myeloid leukemia with t(6;11)(q27;q23): results from Cancer and Leukemia Group B Study 8461 and review of the literature.

C. Bloomfield, R. Larson, K. Mrózek, 2004, Cancer.

Two Distinct Subsets of dic(9;12)(p12;p11.2) among Children with B-Cell Precursor Acute Lymphoblastic Leukemia (ALL): PAX5-ETV6 and ETV6-RUNX1 Rearrangements: A Report from the Children’s Oncology Group.

J. Gastier-Foster, N. Heerema, S. Patil, 2007 .

Cytogenetic heteromorphisms: survey results and reporting practices of giemsa-band regions that we have pondered for years.

S. Patil, G. Vance, A. Brothman, 2006, Archives of pathology & laboratory medicine.

Mature B-cell acute lymphoblastic leukemia with associated translocations (14;18)(q32;q21) and (8;9)(q24;p13). A Burkitt variant?

C. Dunphy, Kathleen W. Rao, G. Dent, 2003, Archives of pathology & laboratory medicine.

A clinical report of a patient with two abnormal cell lines: 46,XX,del(21)(q22.1) and 47,XX,+3

S. McCandless, S. Gold, Kathleen W. Rao, 2005, American journal of medical genetics. Part A.

Section E6.1–6.4 of the ACMG technical standards and guidelines: chromosome studies of neoplastic blood and bone marrow–acquired chromosomal abnormalities

N. Heerema, A. Cherry, F. Mikhail, 2016, Genetics in Medicine.

Karyotypic abnormalities associated with Epstein-Barr virus status in classical Hodgkin lymphoma.

W. Sanger, M. Gulley, Steven M. Johnson, 2016, Cancer genetics.

Microarray analysis for constitutional cytogenetic abnormalities

Christa Lese Martin, Lisa G Shaffer, L. Shaffer, 2007, Genetics in Medicine.

Prenatal diagnosis by FISH in a family with Pelizaeus–Merzbacher disease caused by duplication of the PLP gene

K. Woodward, S. Malcolm, Kathleen W. Rao, 1999 .

Tyrosine kinase inhibitor therapy induces remission in a patient with refractory EBF1-PDGFRB-positive acute lymphoblastic leukemia.

C. Mullighan, K. Roberts, M. Hayden, 2013, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

New recurrent balanced translocations in acute myeloid leukemia and myelodysplastic syndromes: Cancer and leukemia group B 8461

C. Bloomfield, K. Mrózek, A. Carroll, 2013, Genes, chromosomes & cancer.

RUNX1 Amplification Increases the Risk for Thrombosis in Children With B-cell Acute Lymphoblastic Leukemia

A. Deal, J. Blatt, Andrew B Smitherman, 2016, Journal of pediatric hematology/oncology.

Androgenetic/biparental mosaicism causes placental mesenchymal dysplasia

C. Livasy, L. Lefebvre, W. Robinson, 2005, Journal of Medical Genetics.

Follicular lymphoma with a burkitt translocation--predictor of an aggressive clinical course: a case report and review of the literature.

P. Voorhees, C. Dunphy, Kathleen W. Rao, 2004, Archives of pathology & laboratory medicine.

Mucoepidermoid carcinoma of the parotid as a secondary malignancy after chemotherapy in a child with neuroblastoma.

C. Zdanski, W. Shockley, Kathleen W. Rao, 2013, Journal of pediatric hematology/oncology.

Multiple congenital malformations in an infant prenatally diagnosed with mosaicism for dup(1q) and del(Xq)

A. Aylsworth, J. Kuller, Kathleen W. Rao, 1996, Clinical genetics.

Adult patients with de novo acute myeloid leukemia and t(9; 11)(p22; q23) have a superior outcome to patients with other translocations involving band 11q23: a cancer and leukemia group B study.

C. Bloomfield, K. Mrózek, R. Mayer, 1997, Blood.