Yao-Shan Fan

发表

Molecular and genomic aberrations in Chlamydophila psittaci negative ocular adnexal marginal zone lymphomas

Sander R. Dubovy, I. Lossos, Y. Natkunam, 2013, American journal of hematology.

A How-to Guide to Building a Robust SARS-CoV-2 Testing Program at a University-Based Health System

D. Parekh, A. Caban-Martinez, S. Nimer, 2020, Academic pathology.

Randomised trial to assess safety and fetal outcome of early and midtrimester amniocentesis

N. Okun, A. Summers, M. Desrochers, 1998, The Lancet.

HER2 FISH classification of equivocal HER2 IHC breast cancers with use of the 2013 ASCO/CAP practice guideline

I. Reis, Wei Zhao, O. Ikpatt, 2016, Breast Cancer Research and Treatment.

Genotype–phenotype analysis of 4q deletion syndrome: Proposal of a critical region

J. Rosenfeld, C. Stevens, C. Curry, 2012, American journal of medical genetics. Part A.

Randomised trial to assess safety and fetal outcome of early and midtrimester amniocentesis

N. Okun, A. Summers, M. Desrochers, 1998, The Lancet.

Usefulness of HGAL and LMO2 Immunohistochemistry in the Identification of Follicular Lymphomas of the Non-Gastric Gastrointestinal Tract

I. Lossos, Y. Natkunam, J. Chapman-Fredricks, 2012, Applied immunohistochemistry & molecular morphology : AIMM.

Frequent detection of parental consanguinity in children with developmental disorders by a combined CGH and SNP microarray

M. Tekin, S. Sacharow, O. Bodamer, 2013, Molecular Cytogenetics.

Comprehensive cytogenetic analysis including multicolor spectral karyotyping and interphase fluorescence in situ hybridization in lymphoma diagnosis. a summary of 154 cases.

Yao-Shan Fan, K. Rizkalla, Yao‐Shan Fan, 2003, Cancer genetics and cytogenetics.

DIAGNOSIS AND TREATMENT OF DIFFUSE LARGE B-CELL LYMPHOMA IN AN ORANGUTAN (PONGO PYGMAEUS)

J. Rosenblatt, C. Cray, S. Clubb, 2014, Journal of zoo and wildlife medicine : official publication of the American Association of Zoo Veterinarians.

Detection of submicroscopic aberrations in patients with unexplained mental retardation by fluorescence in situ hybridization using multiple subtelomeric probes

V. Siu, M. Speevak, S. Farrell, 2001, Genetics in Medicine.

A 420 Kb Deletion within the Minimum Critical Region of the 15q24 Microdeletion Syndrome in a Female Infant

Yao-Shan Fan, D. Li, Yao‐Shan Fan, 2014 .

Familial 16q24.3 microdeletion involving ANKRD11 causes a KBG‐like syndrome

M. Tekin, S. Sacharow, Yao-Shan Fan, 2012, American journal of medical genetics. Part A.

Screening of deafness-causing DNA variants that are common in patients of European ancestry using a microarray-based approach

M. Tekin, C. Morton, X. Liu, 2017, PloS one.

High‐density array comparative genomic hybridization analysis and follow‐up of a child with a de novo complex chromosome rearrangement detected prenatally

Taosheng Huang, Yao-Shan Fan, A. Vaglio, 2007, Prenatal diagnosis.

Co-existence of other copy number variations with 22q11.2 deletion or duplication: a modifier for variable phenotypes of the syndrome?

M. Tekin, Yao-Shan Fan, M. Tekin, 2012, Molecular Cytogenetics.

Diagnostic application of cyclin D1 fluorescent in situ hybridization for histologically undetermined early lesions of acral melanoma in situ: A case series.

J. Grichnik, G. Elgart, J. Ledon, 2020, Annals of diagnostic pathology.