M. Micale

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Biclonal splenic marginal zone lymphoma with T cell-rich background and aggressive transformation to large cell lymphoma

Marc D. Smith, Alia Gupta, Amy P Gabbard, 2019, Journal of Hematopathology.

Transformation of double-hit large B-cell lymphoma into B-lymphoblastic lymphoma: a case report

A. Glazyrin, M. Micale, James Z. Huang, 2011 .

Defining the extent and nature of cytogenetic events in prostatic adenocarcinoma: paraffin FISH vs. metaphase analysis.

W. Sakr, I. Powell, S. Wolman, 1993, Cancer genetics and cytogenetics.

Prenatal identification of two discontinuous maternally inherited chromosome 7q36.3 microduplications totaling 507 kb including the sonic hedgehog gene in a fetus with multiple congenital anomalies

M. Micale, Bedford Embrey, Katie Hubbell, 2017, Clinical case reports.

An Approach to Definition of Genetic Alterations in Prostate Cancer

W. Sakr, J. Macoska, S. Wolman, 1992, Diagnostic molecular pathology : the American journal of surgical pathology, part B.

Composite Biclonal Marginal Zone Lymphoma of Lung and Chronic Lymphocytic Leukemia: Pathologic, Phenotypic, Cytogenetic, and Molecular Study

M. Micale, V. Douglas-Nikitin, A. M. Blenc, 2011, International journal of surgical pathology.

Constitutional 560.49 kb chromosome 2p24.3 duplication including the MYCN gene identified by SNP chromosome microarray analysis in a child with multiple congenital anomalies and bilateral Wilms tumor.

M. Micale, D. Aughton, Jacqueline K. Macknis, 2016, European journal of medical genetics.

Macrocerebellum, epilepsy, intellectual disability, and gut malrotation in a child with a 16q24.1–q24.2 contiguous gene deletion

Donna M. Martin, B. Foerster, Andrea Seeley, 2014, American journal of medical genetics. Part A.

A multicenter investigation with interphase fluorescence in situ hybridization using X- and Y-chromosome probes.

S. Schwartz, A. Zinsmeister, G. Vance, 1998, American journal of medical genetics.

I. Jaiyesimi, Govinda R Brahmanday, M. Chisti, 2011 .

A multicenter investigation with D-FISH BCR/ABL1 probes.

S. Schwartz, G. Dewald, L. Oseth, 2000, Cancer genetics and cytogenetics.

Xenografts of primary human prostatic carcinoma.

M. Resnick, T. P. Pretlow, E. Kursh, 1993, Journal of the National Cancer Institute.

Extensive genetic alterations in prostate cancer revealed by dual PCR and FISH analysis

W. Sakr, J. Macoska, S. Wolman, 1993, Genes, chromosomes & cancer.

Malignant blue nevus with lymph node metastases

J. Xue, M. Micale, J. Thomas, 2008, Journal of cutaneous pathology.

Chromosomal aneuploidy in proliferative breast disease.

D. Visscher, S. Gulino, S. Wolman, 1994, Human pathology.

Chromosome breakage hotspots and delineation of the critical region for the 9p-deletion syndrome.

S. Schwartz, L. Christ, J. Conroy, 1999, American journal of human genetics.

Mutations in CEP57 cause mosaic variegated aneuploidy syndrome

N. Rahman, D. Gisselsson, J. Clayton-Smith, 2011, Nature Genetics.

Preparation of Amniocytes for Interphase Fluorescence In Situ Hybridization (FISH)

S. Schwartz, M. Micale, L. Becker, 1995, Current protocols in human genetics.

MLL ( myeloid lymphoid lineage or mixed lineage leukemia )

M. Micale, 2017 .

Molecular Cytogenetic (FISH) Analysis of Hematolymphoid Disorders

A. Mohamed, M. Micale, 2012 .

Classical and Molecular Cytogenetic Analysis of Hematolymphoid Disorders

M. Micale, 2011 .

Double trisomy revisited—a multicenter experience

D. V. Van Dyke, A. Adeyinka, M. Micale, 2010, Prenatal diagnosis.

Unusual Presentation of a Small-Cell Variant of Anaplastic Large-Cell Lymphoma Case: When a Septic Picture Is Not Sepsis

I. Jaiyesimi, M. Micale, James Z. Huang, 2017, Case reports in hematology.

Pathological and biological relevance of cytophotometric DNA content to breast carcinoma genetic progression

D. Visscher, J. Crissman, M. Micale, 1993, Journal of cellular biochemistry. Supplement.

Primary Bone Diffuse Large B-cell Lymphoma: Clinicopathologic Study of 21 Cases and Review of Literature

K. Fu, M. Micale, S. Bhagavathi, 2009, The American journal of surgical pathology.

Potential role of biofilms in deep cervical abscess.

A. Sheyn, J. Coticchia, Priyanka Shah, 2014, International journal of pediatric otorhinolaryngology.

Cytogenetics of primary prostatic adenocarcinoma. Clonality and chromosome instability.

W. Sakr, I. Powell, S. Wolman, 1992, Cancer genetics and cytogenetics.

Occult subtotal cleft of the secondary palate with VPI associated to 8q22.2 deletion.

P. Ysunza, M. Micale, Matthew Rontal, 2019, International journal of pediatric otorhinolaryngology.

22q11.2 deletion detected by endoscopic observation of pharyngeal pulsations in a child with submucous cleft palate and persistent velopharyngeal insufficiency.

A. Ysunza, K. Chaiyasate, D. Bloom, 2014, International journal of pediatric otorhinolaryngology.

Velopharyngeal insufficiency, submucous cleft palate and a phonological disorder as the associated clinical features which led to the diagnosis of Jacobsen syndrome. Case report and review of the literature.

A. Ysunza, R. Merson, K. Shaheen, 2013, International journal of pediatric otorhinolaryngology.

ALK-negative anaplastic large T-cell lymphoma with a complex karyotype and DUSP22 gene rearrangement

D. Crisan, M. Micale, Kristle L. Haberichter, 2016 .

Parental origin of De Novo chromosome 9 deletions in del(9p) syndrome.

S. Schwartz, J. Conroy, J. Haren, 1995, American journal of medical genetics.

Mosaic variegated aneuploidy without microcephaly: Implications for cytogenetic diagnosis

N. Rahman, T. Kurczynski, D. V. Van Dyke, 2007, American journal of medical genetics. Part A.

Fluorescence in situ hybridization analysis on cytologic smears: An accurate and efficient method in the diagnosis of melanotic Xp11 translocation renal cancer

Kurt D. Bernacki, Alia Gupta, M. Micale, 2018, Diagnostic cytopathology.

The impact of maternal serum screening programs for Down syndrome in southeast Michigan, 1988–2003

S. Ebrahim, A. Wiktor, M. Micale, 2007, Prenatal diagnosis.

Pediatric T-Cell Acute Lymphoblastic Leukemia

M. Micale, 2018, Atlas of Genetics and Cytogenetics in Oncology and Haematology.

Langerhans/dendritic cell sarcoma arising from hairy cell leukemia: a rare phenomenon

I. Jaiyesimi, M. Chisti, A. Muslimani, 2012, Annals of Hematology.

CYTOGENETIC AND MOLECULAR GENETIC CHARACTERIZATION OF TRISOMY 20 MOSAICISM IN FETAL BLOOD AND TISSUES

John M. Conroy, S. Schwartz, R. Redline, 1996, Prenatal diagnosis.

Secondary acute myelogenous leukemia (AML) with trisomy 10 and del(9q) following precursor B-cell acute lymphoblastic leukemia (ALL) with a hyperdiploid karyotype.

S. Jamil, R. Mody, M. Micale, 2012, Cancer genetics.

Composite Biclonal Marginal Zone Lymphoma of Lung and Chronic Lymphocytic Leukemia: Pathologic, Phenotypic, Cytogenetic, and Molecular Study

M. Micale, A. M. Blenc, S. Bhagavathi, 2011, International journal of surgical pathology.