S. Sheldon

发表

S. Telian, S. Gebarski, A. Griffith, 1998, The Laryngoscope.

Ki-1 anaplastic large cell lymphoma with a prominent leukemic phase.

C. Ross, T. Singleton, M. Anderson, 1996, Human pathology.

Chromosomal aneuploidy in leukemic blast crisis: a potential source of error in interpretation of bone marrow engraftment analysis by VNTR amplification.

A. Killeen, S. Sheldon, N. Akel, 1999, Molecular diagnosis : a journal devoted to the understanding of human disease through the clinical application of molecular biology.

Cytogenetic abnormalities and therapy-related myelodysplastic syndromes in rheumatic disease.

C. Ross, W. Mccune, C. McCarthy, 1998, Arthritis and rheumatism.

Gamma/delta T-cell posttransplantation lymphoproliferative disorder primarily in the spleen.

C. Ross, C. Hanson, B. Schnitzer, 1994, American journal of clinical pathology.

Inflammatory myofibroblastic tumor: cytogenetic evidence supporting clonal origin.

J. Fletcher, S. Weiss, L. Su, 1998, Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc.

Familial Large Vestibular Aqueduct Syndrome

N. Shepard, S. Gebarski, A. Griffith, 1996, The Laryngoscope.

Mapping of the gene for interferon‐inducible dsRNA‐dependent protein kinase to chromosome region 2p21‐22: A site of rearrangements in myeloproliferative disorders

S. Hanash, N. Sonenberg, T. Glover, 1993, Genes, chromosomes & cancer.

Fluorescent In Situ Hybridization

S. Sheldon, 2001 .

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

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

Fluorescent in situ hybridization : evaluation for ploidy and gene amplification.

S. Sheldon, 2001, Methods in molecular medicine.

Differential susceptibility of two cell types to the chromosome-breaking effects of adenovirus type 5.

W. W. Nichols, A. Levan, L. Kjellén, 1971, Mutation research.

A new translocation, t(3;6)(q12;24) associated with chronic myelomonocytic leukaemia and marrow fibrosis.

K. Krishnan, S. Sheldon, 2010, Clinical and laboratory haematology.

DP reactive antibody in a zero mismatch renal transplant pair.

P. Cano, M. Fernandez-Vina, S. Vaidya, 2007, Human immunology.

XY sex reversal and gonadal dysgenesis due to 9p24 monosomy.

M. McDonald, W. Flejter, J. Gorski, 1997, American journal of medical genetics.

Continued presence of nucleoli in human germ cell tumors during mitosis.

J. Lehman, S. Sheldon, 1981, Cancer research.

Nucleolar persistence in embryonal carcinoma cells.

J. Lehman, S. Sheldon, W. Speers, 1981, Experimental cell research.

Cytogenetic and molecular analysis of inv dup(15) chromosomes observed in two patients with autistic disorder and mental retardation.

M. McDonald, W. Flejter, M. Ghaziuddin, 1996, American journal of medical genetics.

A comparison of enzyme-linked immunoabsorbent assays and flow cytometry techniques for the detection of HLA specific antibodies.

J. Worthington, S. Sheldon, S. Martin, 2001, Human immunology.

CHARGE association with choanal atresia and inner ear hypoplasia in a child with a de novo chromosome translocation t(2;7)(p14;q21.11).

D. M. Martin, J. Gorski, S. Sheldon, 2001, American journal of medical genetics.

Chromosomes in autism and related pervasive developmental disorders: a cytogenetic study.

M. Ghaziuddin, E. Weidmer-Mikhail, S. Sheldon, 1998, Journal of intellectual disability research : JIDR.

Unbalanced 5;16 translocation in a boy with papillary thyroid carcinoma.

M. McDonald, J. Innis, S. Maynard, 1994, American journal of medical genetics.

Exclusion of BMP6 as a candidate gene for cleidocranial dysplasia.

T. Friedman, T. Glover, J. Innis, 1997, American journal of medical genetics.

Acute biphenotypic leukaemia: immunophenotypic and cytogenetic analysis

C. Ross, L. Stoolman, C. Hanson, 1993, British journal of haematology.

Abnormalities of chromosome 18 in a girl with mental retardation and autistic disorder.

N. Alessi, M. Ghaziuddin, L. Tsai, 2008, Journal of intellectual disability research : JIDR.

Comparison of the patterns of chromosomal late replication. I. Human renal epithelium and lung fibroblasts in vitro.

W. W. Nichols, S. Sheldon, 1981, Cytogenetics and Cell Genetics.

Autism associated with tetrasomy 15: A further report

M. Ghaziuddin, L. Tsai, N. Ghaziuddin, 1993, European Child & Adolescent Psychiatry.

Autism Associated A Further Report with Tetrasomy 15

L. Tsai, S. Sheldon, S. Venkataraman, 1993 .

Discordant phenotype of two overlapping deletions involving the PAX3 gene in chromosome 2q35.

B. Trask, J. Gorski, S. Sheldon, 1993, Human molecular genetics.

Detection of Philadelphia chromosome-positive cells from glass slide smears using the polymerase chain reaction.

C. Hanson, M. Roth, B. Schnitzer, 1990, The American journal of pathology.

Result of the chromosomal anomaly

E. Thiel, R. Reinhardt, S. Duensing, 2010 .

K. Krishnan, L. Dabich, P. Adams, 2008, Clinical and Laboratory Haematology.