Lista de obras - Gail H. Vance - Dominio Público Uruguay

A 37-year-old man with a pleural mass

artículo científico publicado en 2005

A case of de novo partial tetrasomy of distal 6p and review of the literature

artículo científico publicado en 2007

A report of three patients with an interstitial deletion of chromosome 15q24.

artículo científico publicado en 2005

AML1-FOG2 fusion protein in myelodysplasia

artículo científico publicado en 2005

Acute graft-versus-host disease of the lung after liver transplantation

artículo científico publicado en 2002

Acute panmyelosis with myelofibrosis: an entity distinct from acute megakaryoblastic leukemia

artículo científico publicado en 2005

AluY-mediated germline deletion, duplication and somatic stem cell reversion in UBE2T defines a new subtype of Fanconi anemia.

artículo científico publicado en 2015

American Society of Clinical Oncology/College of American Pathologists guideline recommendations for human epidermal growth factor receptor 2 testing in breast cancer

artículo científico publicado en 2006

American Society of Clinical Oncology/College of American Pathologists guideline recommendations for human epidermal growth factor receptor 2 testing in breast cancer.

artículo científico publicado en 2007

An Adolescent with a Rare De Novo Distal Trisomy 6p and Distal Monosomy 6q Chromosomal Combination

scientific article published on 31 August 2020

Characterization of gains, losses, and regional amplification in testicular germ cell tumor cell lines by comparative genomic hybridization.

artículo científico publicado en 2004

Chronic lymphocytic leukemia/small lymphocytic lymphoma with trisomy 12 and focal cyclin d1 expression: a potential diagnostic pitfall

scientific article published on 01 January 2005

Chronic myelomonocytic leukemia: The role of bone marrow biopsy immunohistology

artículo científico publicado en 2006

Clinical laboratory reports in molecular pathology

artículo científico publicado en 2007

Clinical outcome and follow-up of the first reported case of Russell-Silver syndrome with the unique combination of maternal uniparental heterodisomy 7 and mosaic trisomy 7.

artículo científico publicado en 2005

College of american pathologists proposal for the oversight of laboratory-developed tests

artículo científico publicado en 2011

Combined DOG1 and Mammaglobin Immunohistochemistry Is Comparable to ETV6-breakapart Analysis for Differentiating Between Papillary Cystic Variants of Acinic Cell Carcinoma and Mammary Analogue Secretory Carcinoma

artículo científico publicado en 2016

Complementation of hypersensitivity to DNA interstrand crosslinking agents demonstrates that XRCC2 is a Fanconi anaemia gene

artículo científico publicado en 2016

Cyclophosphamide/fludarabine nonmyeloablative allotransplant for acute myeloid leukemia

artículo científico publicado en 2015

Cytogenetic heteromorphisms: survey results and reporting practices of giemsa-band regions that we have pondered for years.

artículo científico publicado en 2006

Detection of clonal IGH gene rearrangements: summary of molecular oncology surveys of the College of American Pathologists.

artículo científico publicado en 2007

Detection of recurrent cytogenetic abnormalities in acute lymphoblastic and myeloid leukemias using fluorescence in situ hybridization

artículo científico publicado en 2013

Duplication of 18q21.32-q22.3 identified in a stillborn and two relatives with minimal dysmorphic features

artículo científico publicado en 2012

Establishment and characterization of a novel cell line derived from human thymoma AB tumor

artículo científico publicado en 2012

Evaluating current policy for detecting mosaicism in amniotic fluid cultures: implications for current cell counting practices

artículo científico publicado en 2005

Expanding the genotype-phenotype correlation in subtelomeric 19p13.3 microdeletions using high resolution clinical chromosomal microarray analysis.

artículo científico publicado en 2013

FDA's draft guidance on laboratory-developed tests increases clinical and economic risk to adoption of pharmacogenetic testing

artículo científico publicado en 2015

Fluorescence in situ hybridization (FISH) as an aid for the diagnosis of graft-versus-host disease in two multivisceral organ transplant patients

artículo científico publicado en 2013

Genetic disruption of both Fancc and Fancg in mice recapitulates the hematopoietic manifestations of Fanconi anemia.

artículo científico publicado en 2010

Genetic heterogeneity in HER2 testing in breast cancer: panel summary and guidelines

artículo científico publicado en 2009

Genital anomalies in three male siblings with Simpson-Golabi-Behmel syndrome

scientific article published on 01 November 2009

Genome-Wide Association Studies for Taxane-Induced Peripheral Neuropathy in ECOG-5103 and ECOG-1199.

artículo científico publicado en 2015

Glioblastoma occurring at the site of a previous medulloblastoma following a 5-year remission period

artículo científico publicado en 2011

Human Epidermal Growth Factor Receptor 2 Testing in Breast Cancer: American Society of Clinical Oncology/College of American Pathologists Clinical Practice Guideline Focused Update

article

Human Epidermal Growth Factor Receptor 2 Testing in Breast Cancer: American Society of Clinical Oncology/College of American Pathologists Clinical Practice Guideline Focused Update

scholarly article

Hydranencephaly in a newborn with a FLVCR2 mutation and prenatal exposure to cocaine

artículo científico publicado en 2014

Independent Prognostic Significance of Monosomy 17 and Impact of Karyotype Complexity in Monosomal Karyotype/Complex Karyotype Acute Myeloid Leukemia: Results from Four ECOG-ACRIN Prospective Therapeutic Trials

artículo científico publicado en 2017

Interphase FISH demonstrates that human adipose stromal cells maintain a high level of genomic stability in long-term culture

artículo científico publicado en 2009

Karyotype is an independent prognostic factor in adult acute lymphoblastic leukemia (ALL): analysis of cytogenetic data from patients treated on the Medical Research Council (MRC) UKALLXII/Eastern Cooperative Oncology Group (ECOG) 2993 trial

artículo científico publicado en 2006

Large cell carcinoma of the lung mimicking a germ cell tumor: the potential value of chromosome analysis

scientific article published on 12 April 2005

Luminal Subtypes Predict Improved Survival Following Central Nervous System Metastasis in Patients With Surgically Managed Metastatic Breast Carcinoma

artículo científico publicado en 2014

Molecular genetic tests for FLT3, NPM1, and CEBPA in acute myeloid leukemia

artículo científico publicado en 2013

Most primary central nervous system diffuse large B-cell lymphomas occurring in immunocompetent individuals belong to the nongerminal center subtype: a retrospective analysis of 31 cases

article

Novel phenotype of 5p13.3-q11.2 duplication resulting from supernumerary marker chromosome 5: implications for management and genetic counseling.

artículo científico publicado en 2018

Partial trisomy 2q: report of a patient with dup (2)(q33.1q35).

artículo científico publicado en 2005

Phenotypic variability in trisomy 13 mosaicism: two new patients and literature review

scientific article published on 01 June 2009

Positive and negative professionalism experiences of genetic counseling students in the United States and Canada

scientific article published on 03 October 2020

Positive cell-free fetal DNA testing for trisomy 13 reveals confined placental mosaicism

artículo científico publicado en 2013

Preanalytics and Precision Pathology: Pathology Practices to Ensure Molecular Integrity of Cancer Patient Biospecimens for Precision Medicine

scientific article published on 22 July 2019

Pretransplant HLA typing revealed loss of heterozygosity in the major histocompatibility complex in a patient with acute myeloid leukemia

scientific article published on 19 February 2019

Prevalence of maternal cell contamination in amniotic fluid samples.

artículo científico publicado en 2016

Problems with ISCN FISH Nomenclature make it not practical for use in clinical test reports or cytogenetic databases [corrected].

artículo científico publicado en 2003

Proficiency testing for laboratories performing fluorescence in situ hybridization with chromosome-specific DNA probes

artículo científico publicado en 2002

Prognostic and predictive value of tumor vascular endothelial growth factor gene amplification in metastatic breast cancer treated with paclitaxel with and without bevacizumab; results from ECOG 2100 trial

artículo científico publicado en 2013

Prognostic relevance of integrated genetic profiling in acute myeloid leukemia

artículo científico publicado en 2012

Rapid quantification of underivatized alloisoleucine and argininosuccinate using mixed-mode chromatography with tandem mass spectrometry

scientific article published on 05 September 2019

Recommendations for human epidermal growth factor receptor 2 testing in breast cancer: American Society of Clinical Oncology/College of American Pathologists clinical practice guideline update

artículo científico publicado en 2013

Recommendations for human epidermal growth factor receptor 2 testing in breast cancer: American Society of Clinical Oncology/College of American Pathologists clinical practice guideline update

article

Referral patterns of Indiana oncologists for colorectal cancer genetic services

artículo científico publicado en 2010

Reply to E.A. Rakha et al.

artículo científico publicado en 2015

Report of new haplotype for ABCC2 gene: rs17222723 and rs8187718 in cis

artículo científico publicado en 2014

Secondary leukemias in refractory germ cell tumor patients undergoing autologous stem-cell transplantation using high-dose etoposide

artículo científico publicado en 2004

Signet-ring cell lymphoma: clinicopathologic, immunohistochemical, and fluorescence in situ hybridization studies of 7 cases

artículo científico publicado en 2016

The embryonic stem cell transcription factors Oct-4 and FoxD3 interact to regulate endodermal-specific promoter expression.

artículo científico publicado en 2002

Therapy-related myeloid neoplasm with bone marrow involvement, myelosarcoma, and a t(8;16)(p11.2;p13.3)-a case report

artículo científico publicado en 2014

Turner Syndrome (45x) with Clitoromegaly ⬇️

artículo científico publicado el 1 de octubre de 2003

Update on late relapse of germ cell tumor: a clinical and molecular analysis

artículo científico publicado en 2003

Utility of interphase FISH to stratify patients into cytogenetic risk categories at diagnosis of AML in an Eastern Cooperative Oncology Group (ECOG) clinical trial (E1900)

scientific article published on 22 September 2006

Validation of Scales to Measure Benefits of and Barriers to Colorectal Cancer Screening

artículo científico publicado en 2001

Lista de obras de Gail H. Vance

A 37-year-old man with a pleural mass

A case of de novo partial tetrasomy of distal 6p and review of the literature

A report of three patients with an interstitial deletion of chromosome 15q24.

AML1-FOG2 fusion protein in myelodysplasia

Acute graft-versus-host disease of the lung after liver transplantation

Acute panmyelosis with myelofibrosis: an entity distinct from acute megakaryoblastic leukemia

AluY-mediated germline deletion, duplication and somatic stem cell reversion in UBE2T defines a new subtype of Fanconi anemia.

American Society of Clinical Oncology/College of American Pathologists guideline recommendations for human epidermal growth factor receptor 2 testing in breast cancer

American Society of Clinical Oncology/College of American Pathologists guideline recommendations for human epidermal growth factor receptor 2 testing in breast cancer.

An Adolescent with a Rare De Novo Distal Trisomy 6p and Distal Monosomy 6q Chromosomal Combination

Characterization of gains, losses, and regional amplification in testicular germ cell tumor cell lines by comparative genomic hybridization.

Chronic lymphocytic leukemia/small lymphocytic lymphoma with trisomy 12 and focal cyclin d1 expression: a potential diagnostic pitfall

Chronic myelomonocytic leukemia: The role of bone marrow biopsy immunohistology

Clinical laboratory reports in molecular pathology

Clinical outcome and follow-up of the first reported case of Russell-Silver syndrome with the unique combination of maternal uniparental heterodisomy 7 and mosaic trisomy 7.

College of american pathologists proposal for the oversight of laboratory-developed tests

Combined DOG1 and Mammaglobin Immunohistochemistry Is Comparable to ETV6-breakapart Analysis for Differentiating Between Papillary Cystic Variants of Acinic Cell Carcinoma and Mammary Analogue Secretory Carcinoma

Complementation of hypersensitivity to DNA interstrand crosslinking agents demonstrates that XRCC2 is a Fanconi anaemia gene

Cyclophosphamide/fludarabine nonmyeloablative allotransplant for acute myeloid leukemia

Cytogenetic heteromorphisms: survey results and reporting practices of giemsa-band regions that we have pondered for years.

Detection of clonal IGH gene rearrangements: summary of molecular oncology surveys of the College of American Pathologists.

Detection of recurrent cytogenetic abnormalities in acute lymphoblastic and myeloid leukemias using fluorescence in situ hybridization

Duplication of 18q21.32-q22.3 identified in a stillborn and two relatives with minimal dysmorphic features

Establishment and characterization of a novel cell line derived from human thymoma AB tumor

Evaluating current policy for detecting mosaicism in amniotic fluid cultures: implications for current cell counting practices

Expanding the genotype-phenotype correlation in subtelomeric 19p13.3 microdeletions using high resolution clinical chromosomal microarray analysis.

FDA's draft guidance on laboratory-developed tests increases clinical and economic risk to adoption of pharmacogenetic testing

Fluorescence in situ hybridization (FISH) as an aid for the diagnosis of graft-versus-host disease in two multivisceral organ transplant patients

Genetic disruption of both Fancc and Fancg in mice recapitulates the hematopoietic manifestations of Fanconi anemia.

Genetic heterogeneity in HER2 testing in breast cancer: panel summary and guidelines

Genital anomalies in three male siblings with Simpson-Golabi-Behmel syndrome

Genome-Wide Association Studies for Taxane-Induced Peripheral Neuropathy in ECOG-5103 and ECOG-1199.

Glioblastoma occurring at the site of a previous medulloblastoma following a 5-year remission period

Human Epidermal Growth Factor Receptor 2 Testing in Breast Cancer: American Society of Clinical Oncology/College of American Pathologists Clinical Practice Guideline Focused Update

Human Epidermal Growth Factor Receptor 2 Testing in Breast Cancer: American Society of Clinical Oncology/College of American Pathologists Clinical Practice Guideline Focused Update

Hydranencephaly in a newborn with a FLVCR2 mutation and prenatal exposure to cocaine

Independent Prognostic Significance of Monosomy 17 and Impact of Karyotype Complexity in Monosomal Karyotype/Complex Karyotype Acute Myeloid Leukemia: Results from Four ECOG-ACRIN Prospective Therapeutic Trials

Interphase FISH demonstrates that human adipose stromal cells maintain a high level of genomic stability in long-term culture

Karyotype is an independent prognostic factor in adult acute lymphoblastic leukemia (ALL): analysis of cytogenetic data from patients treated on the Medical Research Council (MRC) UKALLXII/Eastern Cooperative Oncology Group (ECOG) 2993 trial

Large cell carcinoma of the lung mimicking a germ cell tumor: the potential value of chromosome analysis

Luminal Subtypes Predict Improved Survival Following Central Nervous System Metastasis in Patients With Surgically Managed Metastatic Breast Carcinoma

Molecular genetic tests for FLT3, NPM1, and CEBPA in acute myeloid leukemia

Most primary central nervous system diffuse large B-cell lymphomas occurring in immunocompetent individuals belong to the nongerminal center subtype: a retrospective analysis of 31 cases

Novel phenotype of 5p13.3-q11.2 duplication resulting from supernumerary marker chromosome 5: implications for management and genetic counseling.

Partial trisomy 2q: report of a patient with dup (2)(q33.1q35).

Phenotypic variability in trisomy 13 mosaicism: two new patients and literature review

Positive and negative professionalism experiences of genetic counseling students in the United States and Canada

Positive cell-free fetal DNA testing for trisomy 13 reveals confined placental mosaicism

Preanalytics and Precision Pathology: Pathology Practices to Ensure Molecular Integrity of Cancer Patient Biospecimens for Precision Medicine

Pretransplant HLA typing revealed loss of heterozygosity in the major histocompatibility complex in a patient with acute myeloid leukemia

Prevalence of maternal cell contamination in amniotic fluid samples.

Problems with ISCN FISH Nomenclature make it not practical for use in clinical test reports or cytogenetic databases [corrected].

Proficiency testing for laboratories performing fluorescence in situ hybridization with chromosome-specific DNA probes

Prognostic and predictive value of tumor vascular endothelial growth factor gene amplification in metastatic breast cancer treated with paclitaxel with and without bevacizumab; results from ECOG 2100 trial

Prognostic relevance of integrated genetic profiling in acute myeloid leukemia

Rapid quantification of underivatized alloisoleucine and argininosuccinate using mixed-mode chromatography with tandem mass spectrometry

Recommendations for human epidermal growth factor receptor 2 testing in breast cancer: American Society of Clinical Oncology/College of American Pathologists clinical practice guideline update

Recommendations for human epidermal growth factor receptor 2 testing in breast cancer: American Society of Clinical Oncology/College of American Pathologists clinical practice guideline update

Referral patterns of Indiana oncologists for colorectal cancer genetic services

Reply to E.A. Rakha et al.

Report of new haplotype for ABCC2 gene: rs17222723 and rs8187718 in cis

Secondary leukemias in refractory germ cell tumor patients undergoing autologous stem-cell transplantation using high-dose etoposide

Signet-ring cell lymphoma: clinicopathologic, immunohistochemical, and fluorescence in situ hybridization studies of 7 cases

The embryonic stem cell transcription factors Oct-4 and FoxD3 interact to regulate endodermal-specific promoter expression.

Therapy-related myeloid neoplasm with bone marrow involvement, myelosarcoma, and a t(8;16)(p11.2;p13.3)-a case report

Turner Syndrome (45x) with Clitoromegaly ⬇️

Update on late relapse of germ cell tumor: a clinical and molecular analysis

Utility of interphase FISH to stratify patients into cytogenetic risk categories at diagnosis of AML in an Eastern Cooperative Oncology Group (ECOG) clinical trial (E1900)

Validation of Scales to Measure Benefits of and Barriers to Colorectal Cancer Screening