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Genotype-phenotype analysis of 4q deletion syndrome: Proposal of a critical region.
Published in:
American Journal of Medical Genetics. Part A, 2012, v. 158A, n. 9, p. 2139, doi. 10.1002/ajmg.a.35502
By:
- Strehle, Eugen-Matthias;
- Yu, Linbo;
- Rosenfeld, Jill A.;
- Donkervoort, Sandra;
- Zhou, Yulin;
- Chen, Tian-Jian;
- Martinez, Jose E.;
- Fan, Yao-Shan;
- Barbouth, Deborah;
- Zhu, Hongbo;
- Vaglio, Alicia;
- Smith, Rosemarie;
- Stevens, Cathy A.;
- Curry, Cynthia J.;
- Ladda, Roger L.;
- Fan, Zheng (Jane);
- Fox, Joyce E.;
- Martin, Judith A.;
- Abdel-Hamid, Hoda Z.;
- McCracken, Elizabeth A.
Publication type:
Article
Familial 16q24.3 microdeletion involving ANKRD11 causes a KBG-like syndrome.
Published in:
American Journal of Medical Genetics. Part A, 2012, v. 158A, n. 3, p. 547, doi. 10.1002/ajmg.a.34436
By:
- Sacharow, Stephanie;
- Li, Deling;
- Fan, Yao Shan;
- Tekin, Mustafa
Publication type:
Article
Cytogenetic aspects of the Canadian early and mid-trimester amniotic fluid trial (CEMAT).
Published in:
1999
By:
- Winsor, Elizabeth J. T.;
- Tomkins, Darrell J.;
- Kalousek, Dagmar;
- Farrell, Sandra;
- Wyatt, Philip;
- Fan, Yao-Shan;
- Carter, Ronald;
- Wang, Hungshu;
- Dallaire, Louis;
- Eydoux, Patrice;
- Welch, J. Philip;
- Dawson, Angelika;
- Lin, Jim C. C.;
- Singer, Joel;
- Johnson, JoAnn;
- Wilson, R. Douglas;
- Winsor, E J;
- Tomkins, D J;
- Kalousek, D;
- Farrell, S
Publication type:
journal article
Fetal nuchal oedema and antenatal diagnosis of trisomy 10.
Published in:
Prenatal Diagnosis, 1994, v. 14, n. 6, p. 463, doi. 10.1002/pd.1970140609
By:
- Farrell, S. A.;
- Sue-Chue-Lam, A.;
- Miskin, M.;
- Fan, Yao-Shan
Publication type:
Article
Brief Report: A Case of Autism with Interstitial Deletion of Chromosome 13.
Published in:
2001
By:
- Steele, Margaret Mary;
- Al-Adeimi, Mohammed;
- Mok Siu, Victoria;
- Fan, Yao-Shan
Publication type:
Case Study
Brief Report: An Assessment of Stimulus Generalization and Contingency Effects in Functional Communication Training with Two Students with Autism.
Published in:
Journal of Autism & Developmental Disorders, 2001, v. 31, n. 2, p. 235, doi. 10.1023/A:1010711518182
By:
- O'Neill, Robert E.;
- Sweetland-Baker, Margaret;
- Mok Siu, Victoria;
- Fan, Yao-Shan
Publication type:
Article
Comparison Between Integrated Genomic DNA/RNA Profiling and Fluorescence In Situ Hybridization in the Detection of MYC, BCL-2, and BCL-6 Gene Rearrangements in Large B-Cell Lymphomas.
Published in:
American Journal of Clinical Pathology, 2020, v. 153, n. 3, p. 353, doi. 10.1093/ajcp/aqz172
By:
- Cassidy, Daniel P;
- Chapman, Jennifer R;
- Lopez, Rafael;
- White, Kyle;
- Fan, Yao-Shan;
- Casas, Carmen;
- Severson, Eric A;
- Vega, Francisco
Publication type:
Article
Comparison Between Integrated Genomic DNA/RNA Profiling and Fluorescence In Situ Hybridization in the Detection of MYC, BCL-2, and BCL-6 Gene Rearrangements in Large B-Cell Lymphomas.
Published in:
2019
By:
- Cassidy, Daniel P;
- Chapman, Jennifer R;
- Lopez, Rafael;
- White, Kyle;
- Fan, Yao-Shan;
- Casas, Carmen;
- Severson, Eric A;
- Vega, Francisco
Publication type:
journal article
Primary Mediastinal Large B-Cell Lymphoma With Translocations Involving BCL6 and MYC (Double-Hit Lymphoma).
Published in:
2016
By:
- Campuzano-Zuluaga, Germán;
- Ortiz, Daniel;
- Jing-Hong Peng;
- Ikpatt, Offiong Francis;
- Yao-Shan Fan;
- Barredo, Julio C.;
- Vega, Francisco;
- Chapman, Jennifer R.;
- Peng, Jing-Hong;
- Francis Ikpatt, Offiong;
- Fan, Yao-Shan
Publication type:
journal article
HER2 FISH classification of equivocal HER2 IHC breast cancers with use of the 2013 ASCO/CAP practice guideline.
Published in:
Breast Cancer Research & Treatment, 2016, v. 155, n. 3, p. 457, doi. 10.1007/s10549-016-3717-z
By:
- Fan, Yao-Shan;
- Casas, Carmen;
- Peng, Jinghong;
- Watkins, Melanie;
- Fan, Lynn;
- Chapman, Jennifer;
- Ikpatt, Offiong;
- Gomez, Carmen;
- Zhao, Wei;
- Reis, Isildinha
Publication type:
Article
De novo acute myeloid leukemia with monocytoid blasts and erythrophagocytosis.
Published in:
Clinical Case Reports, 2014, v. 2, n. 6, p. 333, doi. 10.1002/ccr3.120
By:
- Blieden, Clifford;
- Fan, Yao‐Shan;
- Chapman, Jennifer Rose;
- Vega, Francisco
Publication type:
Article
Monosomy chromosome 21 compensated by 21q22.11q22.3 duplication in a case with small size and minor anomalies.
Published in:
Molecular Cytogenetics (17558166), 2018, v. 11, n. 1, p. N.PAG, doi. 10.1186/s13039-018-0390-4
By:
- Su, Meng;
- Benke, Paul J.;
- Bademci, Guney;
- Cengiz, Filiz Basak;
- Ouyang, Xiaomei;
- Peng, Jinghong;
- Casas, Carmen E.;
- Tekin, Mustafa;
- Fan, Yao-Shan
Publication type:
Article
Molecular and genomic aberrations in Chlamydophila psittaci negative ocular adnexal marginal zone lymphomas.
Published in:
American Journal of Hematology, 2013, v. 88, n. 9, p. 730, doi. 10.1002/ajh.23490
By:
- Zhu, Daxing;
- Ikpatt, Offiong F.;
- Dubovy, Sander R.;
- Lossos, Chen;
- Natkunam, Yasodha;
- Chapman-Fredricks, Jennifer R.;
- Fan, Yao-Shan;
- Lossos, Izidore S.
Publication type:
Article
High-density array comparative genomic hybridization analysis and follow-up of a child with a de novo complex chromosome rearrangement detected prenatally.
Published in:
Prenatal Diagnosis, 2007, v. 27, n. 10, p. 982, doi. 10.1002/pd.1831
By:
- Quadrelli, A.;
- Vaglio, A.;
- Quadrelli, R.;
- Mechoso, B.;
- Fan, Yao-Shan;
- Huang, T.
Publication type:
Article
Copy number variant discrepancy resolution using the ClinGen dosage sensitivity map results in updated clinical interpretations in ClinVar.
Published in:
Human Mutation, 2018, v. 39, n. 11, p. 1650, doi. 10.1002/humu.23610
By:
- Riggs, Erin R.;
- Nelson, Tristan;
- Merz, Andrew;
- Ackley, Todd;
- Bunke, Brian;
- Collins, Christin D.;
- Collinson, Morag N.;
- Fan, Yao‐Shan;
- Goodenberger, McKinsey L.;
- Golden, Denae M.;
- Haglund‐Hazy, Linda;
- Krgovic, Danijela;
- Lamb, Allen N.;
- Lewis, Zoe;
- Li, Guang;
- Liu, Yajuan;
- Meck, Jeanne;
- Neufeld‐Kaiser, Whitney;
- Runke, Cassandra K.;
- Sanmann, Jennifer N.
Publication type:
Article
Detection of pathogenic gene copy number variations in patients with mental retardation by genomewide oligonucleotide array comparative genomic hybridization.
Published in:
Human Mutation, 2007, v. 28, n. 11, p. 1124, doi. 10.1002/humu.20581
By:
- Fan, Yao-Shan;
- Jayakar, Parul;
- Zhu, Hongbo;
- Barbouth, Deborah;
- Sacharow, Stephanie;
- Morales, Ana;
- Carver, Virginia;
- Benke, Paul;
- Mundy, Peter;
- Elsas, Louis J.
Publication type:
Article
Endoscopic ultrasound guided fine needle aspiration with fluorescence in situ hybridization analysis in 104 patients with pancreatic mass.
Published in:
Journal of Gastroenterology & Hepatology, 2014, v. 29, n. 8, p. 1654, doi. 10.1111/jgh.12575
By:
- Ribeiro, Afonso;
- Peng, Jinghong;
- Casas, Carmen;
- Fan, Yao‐Shan
Publication type:
Article
Screening of deafness-causing DNA variants that are common in patients of European ancestry using a microarray-based approach.
Published in:
PLoS ONE, 2017, v. 12, n. 3, p. 1, doi. 10.1371/journal.pone.0169219
By:
- Yan, Denise;
- Xiang, Guangxin;
- Chai, Xingping;
- Qing, Jie;
- Shang, Haiqiong;
- Zou, Bing;
- Mittal, Rahul;
- Shen, Jun;
- Smith, Richard J. H.;
- Fan, Yao-Shan;
- Blanton, Susan H.;
- Tekin, Mustafa;
- Morton, Cynthia;
- Xing, Wanli;
- Cheng, Jing;
- Liu, Xue Zhong
Publication type:
Article

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