V. Lindgren

发表

Diagnosis of Angelman syndrome in infants.

W. R. Breg, J. S. Fryburg, V. Lindgren, 1991, American journal of medical genetics.

Do NF1 gene deletions result in a characteristic phenotype?

J. Tonsgard, M. Short, V. Lindgren, 1997, American journal of medical genetics.

Effects of chromatin-modifying agents on CD34+ cells from patients with idiopathic myelofibrosis.

R. Hoffman, Wei Zhang, Wenyang Hu, 2007, Cancer research.

Durable complete remission induced by cetuximab monotherapy in a patient infected with HIV and diagnosed with recurrent squamous cell carcinoma of the head and neck.

S. Setty, M. Yao, J. Radosevich, 2011, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Comparative analysis of mouse-human hybrids with rearranged chromosomes 1 by in situ hybridization and southern blotting: High-resolution mapping of NRAS, NGFB, and AMY on human chromosome 1

U. Francke, V. Lindgren, M. Münke, 1984, Somatic cell and molecular genetics.

Renal tumor with overlapping distal nephron morphology and karyotype.

S. Campbell, M. Picken, G. Paner, 2004, Archives of pathology & laboratory medicine.

A Case of Osteogenesis Imperfecta Type II With Additional Balanced Translocation t(1;20)(p13;p11.2)

R. Emmadi, C. Enakpene, S. Garzon, 2019, Fetal and pediatric pathology.

Intracranial plasmacytoma mimicking meningioma in a patient with Castleman's disease

Yi-Hsiang Chen, S. Abutalib, V. Lindgren, 2009, American journal of hematology.

Human genes involved in cholesterol metabolism: chromosomal mapping of the loci for the low density lipoprotein receptor and 3-hydroxy-3-methylglutaryl-coenzyme A reductase with cDNA probes.

U. Francke, D. Russell, K. Luskey, 1985, Proceedings of the National Academy of Sciences of the United States of America.

The constitutive mobilization of bone marrow-repopulating cells into the peripheral blood in idiopathic myelofibrosis.

N. Mahmud, R. Hoffman, G. Barosi, 2005, Blood.

Human ornithine transcarbamylase locus mapped to band Xp21.1 near the Duchenne muscular dystrophy locus.

U. Francke, A. Horwich, L. Rosenberg, 1984, Science.

Metanephric Adenosarcoma in a Young Adult: Morphologic, Immunophenotypic, Ultrastructural, and Fluorescence In Situ Hybridization Analyses: A Case Report and Review of the Literature

J. Eble, M. Picken, Joseph I. Clark, 2001, The American journal of surgical pathology.

Phenotypic, cytogenetic, and molecular studies of three patients with constitutional deletions of chromosome 5 in the region of the gene for familial adenomatous polyposis.

U. Francke, T. Ozcelik, T. Yang-Feng, 1992, American journal of human genetics.

Structural andTranscriptional Analysis ofHumanPapillomavirus Type16Sequences inCervical Carcinoma CellLines

V. Lindgren, 1987 .

Comprehensive analysis of CBFbeta-MYH11 fusion transcripts in acute myeloid leukemia by RT-PCR analysis.

F. Ravandi, S. Kadkol, C. Dodge, 2004, The Journal of molecular diagnostics : JMD.

The pattern and clinical significance of karyotypic abnormalities in patients with idiopathic and postpolycythemic myelofibrosis

J. Rowley, J. Testa, J. Miller, 1985, Cancer.

Acute myelogenous leukemia with t(6;9)(p23;q34) and marrow basophilia: an overview.

V. Lindgren, S. Gaitonde, Yiqing Chi, 2008, Archives of pathology & laboratory medicine.

Why Do I Still Have a Bruise Around My Knee

D. Rondelli, S. Abutalib, V. Lindgren, 2008 .

Molecular identification of CBFβ-MYH11 fusion transcripts in an AML M4Eo patient in the absence of inv16 or other abnormality by cytogenetic and FISH analyses – a rare occurrence

F. Ravandi, S. Kadkol, C. Dodge, 2003, Leukemia.

Specific chromosomal abnormalities characterize fibrosarcomas of bovine papillomavirus type 1 transgenic mice.

D. Hanahan, P. Howley, J. Skowroński, 1989, Proceedings of the National Academy of Sciences of the United States of America.

Comparable complex rearrangements involving 8;21 and 9;22 translocations in leukaemia

J. Rowley, V. Lindgren, 1977, Nature.

Hairy cell leukemia: An analysis of the chromosomes of 26 patients

J. Rowley, H. Golomb, V. Lindgren, 1978, Virchows Archiv. B, Cell pathology.

Chronic myelomonocytic leukemia with p190 BCR-ABL rearrangement mimicking advanced liver disease at presentation

D. Peace, S. Kadkol, V. Lindgren, 2007, Acta oncologica.

Chromosomal localization of human Na+,K+-ATPase α- and β-subunit genes

U. Francke, J. Lingrel, J. Schneider, 1988 .

Evaluation of Genotoxicity of Chromatin Modifying Agents Expanded Hematopoietic Graft in a Non-Human Primate Model.

N. Mahmud, J. Quigley, D. Rondelli, 2012 .

Autism orAtypical Autism inMaternally butNotPaternally Derived Proximal 15qDuplication

C. Lord, V. Lindgren, 1997 .

Possible Epigenetic Regulation of Functionally Opposing Groups of Genes Involved in Ex Vivo Expansion of Cord Blood Stem Cells

N. Mahmud, V. Lindgren, S. Baluchamy, 2008 .

Chromosome abnormalities in patients with hairy cell leukemia

J. Rowley, H. Golomb, V. Lindgren, 1978, Cancer.

Chromosomal localization of human Na+, K+-ATPase alpha- and beta-subunit genes.

U. Francke, J. Lingrel, J. Schneider, 1988, Genomics.

Structural and transcriptional analysis of human papillomavirus type 16 sequences in cervical carcinoma cell lines

M. Braun, M. Gonda, P. Howley, 1987, Journal of virology.

Description of a flow cytometry approach based on SYBR-14 staining for the assessment of DNA content, cell cycle analysis, and sorting of living normal and neoplastic cells.

R. Nuñez, N. Garay, V. Lindgren, 2004, Experimental and molecular pathology.

Minor Xp21 chromosome deletion in a male associated with expression of Duchenne muscular dystrophy, chronic granulomatous disease, retinitis pigmentosa, and McLeod syndrome.

C. Disteche, U. Francke, H. Ochs, 1985, American journal of human genetics.

Chimerism as the etiology of a 46,XX/46,XY fertile true hermaphrodite.

A. Talerman, C. Ober, A. Amarose, 1992, Fertility and sterility.

Chromosome replication in aging human diploid fibroblasts.

R. Farber, V. Lindgren, 1982, Experimental cell research.

Autism or atypical autism in maternally but not paternally derived proximal 15q duplication.

B. Leventhal, C. Lord, E. Cook, 1997, American journal of human genetics.

Human genes for U2 small nuclear RNA map to a major adenovirus 12 modification site on chromosome 17

M. Ares, A. Weiner, U. Francke, 1985, Nature.

Human U1 small nuclear RNA pseudogenes do not map to the site of the U1 genes in 1p36 but are clustered in 1q12-q22

A. Weiner, U. Francke, L. B. Bernstein, 1985, Molecular and cellular biology.

Human Ul Small Nuclear RNA Pseudogenes Do Not Map to the Site of the Ul Genes in lp36 but Are Clustered in lql2-q22

A. Weiner, U. Francke, L. B. Bernstein, 2022 .

Two patients with overlapping de novo duplications of the long arm of chromosome 9, including one case with Di George sequence.

E. Berry-Kravis, V. Lindgren, B. Rosinsky, 1994, American journal of medical genetics.

Genomic imprinting in disorders of growth.

V. Lindgren, Valerie Lindgren, 1996, Endocrinology and metabolism clinics of North America.

Monosomy 22 in two ovarian granulosa cell tumors.

S. Waggoner, J. Rotmensch, V. Lindgren, 1996, Cancer genetics and cytogenetics.

Cytogenetic analysis of a series of 13 renal oncocytomas.

S. Campbell, A. Omeroglu, M. Picken, 2004, The Journal of urology.

Behavioral abnormalities are common and severe in patients with distal 22q11.2 microdeletions and microduplications

G. Hoganson, R. Dineen, V. Lindgren, 2015, Molecular genetics & genomic medicine.

Temple syndrome resulting from uniparental disomy is undiagnosed by a methylation assay due to low‐level mosaicism for trisomy 14

V. Lindgren, Gifty Bhat, Katherine Cobian, 2021, American journal of medical genetics. Part A.

Unique immunologic patterns in fibromyalgia

F. Behm, Oleksiy Karpenko, I. Gavin, 2012, BMC Clinical Pathology.

der(3)t(3;5). Another recurring abnormality in myelodysplastic disorder.

T. Yang-Feng, V. Lindgren, L. Gibson, 1991, Cancer genetics and cytogenetics.

Passive seeding in metanephric adenoma: a review of pseudometastatic lesions in perinephric lymph nodes.

M. Picken, G. Paner, Joseph I. Clark, 2005, Archives of pathology & laboratory medicine.

Thrombocytopenia and Predisposition to Acute Myeloid Leukemia due to Mosaic Ring 21 with Loss of RUNX1: Cytogenetic and Molecular Characterization

H. Ni, V. Lindgren, M. Schmidt, 2018, Molecular Syndromology.

Cytogenetic and molecular characterization of marker chromosomes in patients with mosaic 45,X karyotypes

D. Page, P. Lichter, Chih-ping Chen, 1992, Human Genetics.

Novel isodicentric chromosome 18 in an abnormal infant with a mosaic karyotype [46,XY/46,XY,-18,+dic(18)(q12.2]).

T. Yang-Feng, J. S. Fryburg, V. Lindgren, 1990, American journal of medical genetics.

Chromosome replication in normal and transformed human lymphocytes.

R. Farber, V. Lindgren, 1983, Cancer genetics and cytogenetics.

Anterior Pituitary Aplasia in an Infant with Ring Chromosome 18p Deletion

V. Lindgren, C. Boucher-Berry, Sarah Durrin, 2016, Case reports in endocrinology.

Acute Myeloid Leukemia With Myelodysplasia- Related Changes A New Entity Defined by the WHO 2008 Classification of Hematopoietic and Lymphoid Neoplasms

J. Quigley, D. Peace, D. Rondelli, 2009 .

Extranodal Natural Killer/T-Cell Lymphoma, Nasal Type, in a Patient with a Constitutional 11q Terminal Deletion Disorder

D. Rondelli, A. Attele, S. Abutalib, 2007, Acta Haematologica.

The Y- autosome ttanslocation ofCallimico goeldii

Susan W. Margulis, J. Dubach, V. Lindgren, 1995, International Journal of Primatology.

High incidence of chromosome 1 abnormalities in a series of 27 renal oncocytomas: cytogenetic and fluorescence in situ hybridization studies.

S. Campbell, M. Picken, G. Paner, 2007, Archives of pathology & laboratory medicine.

MLL-SEPT6 fusion transcript with a novel sequence in an infant with acute myeloid leukemia.

Steven S. Oh, S. Kadkol, V. Lindgren, 2006, Cancer genetics and cytogenetics.

Short communication MLL-SEPT6 fusion transcript with a novel sequence in an infant with acute myeloid leukemia

Steven S. Oh, S. Kadkol, V. Lindgren, 2006 .

Regional assignments of the zinc finger Y-linked gene (ZFY) and related sequences on human and mouse chromosomes.

Y. Lau, V. Lindgren, W. Leung, 1990, Cytogenetics and cell genetics.

The location of chromosome breaks in Bloom's syndrome.

V. Lindgren, 1981, Cytogenetics and cell genetics.

The Principles of Clinical Cytogenetics

V. Lindgren, Joan M. Stoler, 1999, Humana Press.