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Journal Article
The American Journal of Surgical Pathology, ISSN 0147-5185, 09/2015, Volume 39, Issue 9, pp. 1197 - 1205
Ovarian small cell carcinoma of the hypercalcemic type (SCCOHT)/ovarian rhabdoid tumor is a rare and highly malignant tumor that typically occurs in young... 
Rhabdoid tumor | Ovary | INI1/SMARCB1 | SMARCA4/BRG1 | Small cell carcinoma hypercalcemic type | SURGERY | SMARCB1 | FUSION | NEOPLASMS | BRG1 | PATHOLOGY | small cell carcinoma hypercalcemic type | SMARCA4 | INI1 | ovary | SARCOMAS | rhabdoid tumor | MUTATIONS | Immunohistochemistry | Predictive Value of Tests | Carcinoma, Small Cell - genetics | Nuclear Proteins - analysis | Humans | Middle Aged | Ovarian Neoplasms - pathology | Sarcoma, Ewing - pathology | Granulosa Cell Tumor - pathology | Rhabdoid Tumor - pathology | Bone Neoplasms - pathology | Ovarian Neoplasms - genetics | Young Adult | Carcinoma, Small Cell - chemistry | Sarcoma, Endometrial Stromal - pathology | Soft Tissue Neoplasms - chemistry | Melanoma - genetics | Bone Neoplasms - chemistry | Adult | Female | Bone Neoplasms - genetics | Melanoma - chemistry | Soft Tissue Neoplasms - genetics | Hypercalcemia - genetics | Diagnosis, Differential | Ovarian Neoplasms - chemistry | Sarcoma, Ewing - chemistry | Hypercalcemia - pathology | Endometrial Neoplasms - chemistry | Biomarkers, Tumor - analysis | Rhabdoid Tumor - chemistry | Hypercalcemia - metabolism | Melanoma - pathology | Sarcoma, Endometrial Stromal - chemistry | Rhabdoid Tumor - genetics | Biopsy | Adolescent | Soft Tissue Neoplasms - pathology | DNA Helicases - analysis | Endometrial Neoplasms - pathology | Granulosa Cell Tumor - chemistry | Biomarkers, Tumor - genetics | Transcription Factors - analysis | Carcinoma, Small Cell - pathology | Neoplasm Staging | Sarcoma, Ewing - genetics | Index Medicus
Journal Article
Modern Pathology, ISSN 0893-3952, 06/2010, Volume 23, Issue 6, pp. 781 - 789
Journal Article
Gastroenterology, ISSN 0016-5085, 2008, Volume 135, Issue 2, pp. 419 - 428.e1
Background & Aims: Although the clinical phenotype of Lynch syndrome (also known as hereditary nonpolyposis colorectal cancer) has been well described, little... 
Gastroenterology and Hepatology | BETHESDA GUIDELINES | COLON-CANCER | DNA MISMATCH REPAIR | CHILDHOOD-CANCER | NONPOLYPOSIS COLORECTAL-CANCER | MICROSATELLITE INSTABILITY | HETEROZYGOUS MUTATIONS | GASTROENTEROLOGY & HEPATOLOGY | CONSTITUTIVE DEFICIENCY | ENDOMETRIAL CANCER | GENE PMS2 | Immunohistochemistry | Colorectal Neoplasms - genetics | Colorectal Neoplasms, Hereditary Nonpolyposis - pathology | Humans | Middle Aged | DNA Repair Enzymes - genetics | Gene Expression Regulation, Neoplastic | Colorectal Neoplasms - chemistry | DNA-Binding Proteins - analysis | Male | DNA Mutational Analysis - methods | Endometrial Neoplasms - genetics | Ligase Chain Reaction | Adenosine Triphosphatases - analysis | Polymerase Chain Reaction | Germ-Line Mutation | Adult | Female | Mismatch Repair Endonuclease PMS2 | Odds Ratio | Endometrial Neoplasms - chemistry | Risk Assessment | Colorectal Neoplasms, Hereditary Nonpolyposis - genetics | Genotype | Penetrance | DNA-Binding Proteins - genetics | DNA Repair Enzymes - analysis | Phenotype | Proto-Oncogene Proteins B-raf - genetics | Endometrial Neoplasms - pathology | Heterozygote | Adenosine Triphosphatases - genetics | Aged | Colorectal Neoplasms, Hereditary Nonpolyposis - chemistry | Colorectal Neoplasms - pathology | Genetic aspects | Research | Oncology, Experimental | Colorectal cancer | Cancer | Index Medicus | Abridged Index Medicus
Journal Article
The American Journal of Surgical Pathology, ISSN 0147-5185, 02/2016, Volume 40, Issue 2, pp. 166 - 180
Mixed endometrial carcinoma refers to a tumor that comprises 2 or more distinct histotypes. We studied 18 mixed-type endometrial carcinomas—11 mixed serous and... 
Serous carcinoma | Endometrioid carcinoma clear cell carcinoma | Nextgeneration sequencing | Endometrial cancer | Mixed carcinoma | SURGERY | next-generation sequencing | P53 EXPRESSION | PROGNOSIS | endometrioid carcinoma clear cell carcinoma | ADENOCARCINOMAS | mixed carcinoma | CLASSIFICATION | PATHOLOGY | DEFICIENCY | UTERINE SEROUS CARCINOMA | endometrial cancer | DIAGNOSTIC UTILITY | OVARIAN | MUTATIONS | serous carcinoma | CLEAR-CELL CARCINOMA | Immunohistochemistry | Neoplasms, Complex and Mixed - genetics | Predictive Value of Tests | Alberta | Humans | Middle Aged | Carcinoma - chemistry | Neoplasms, Complex and Mixed - therapy | Molecular Diagnostic Techniques | Neoplasm Grading | Endometrial Neoplasms - genetics | Time Factors | DNA Mutational Analysis | Neoplasms, Complex and Mixed - diagnosis | Aged, 80 and over | Female | Carcinoma - pathology | Genetic Predisposition to Disease | Endometrial Neoplasms - chemistry | Biomarkers, Tumor - analysis | Carcinoma - diagnosis | Treatment Outcome | Endometrial Neoplasms - diagnosis | Neoplasms, Complex and Mixed - chemistry | Phenotype | Neoplasms, Complex and Mixed - pathology | Endometrial Neoplasms - therapy | Carcinoma - genetics | Carcinoma - therapy | Endometrial Neoplasms - pathology | Aged | Biomarkers, Tumor - genetics | High-Throughput Nucleotide Sequencing | Mutation | Clonal Evolution | Evolution, Molecular | Index Medicus | next generation sequencing
Journal Article
The American Journal of Surgical Pathology, ISSN 0147-5185, 09/2014, Volume 38, Issue 9, pp. 1173 - 1181
Journal Article
The American Journal of Surgical Pathology, ISSN 0147-5185, 11/2014, Volume 38, Issue 11, pp. 1501 - 1509
Lynch syndrome (LS) is an autosomal dominant inherited disorder caused by germline mutations in DNA mismatch repair (MMR) genes. Mutation carriers are at... 
Microsatellite instability | Endometrial adenocarcinoma | Lynch syndrome | Mismatch-repair deficiency | SURGERY | mismatch-repair deficiency | microsatellite instability | NONPOLYPOSIS COLORECTAL-CANCER | REPAIR PROTEIN IMMUNOHISTOCHEMISTRY | RISK | GENE MUTATION | endometrial adenocarcinoma | PATHOLOGY | CLINICAL-CRITERIA | ACADEMIC-MEDICAL-CENTER | TUMOR MORPHOLOGY | GERMLINE MUTATIONS | GYNECOLOGIC CANCERS | Immunohistochemistry | MutL Protein Homolog 1 | Predictive Value of Tests | Microsatellite Instability | Biomarkers, Tumor - deficiency | Colorectal Neoplasms, Hereditary Nonpolyposis - pathology | Humans | Middle Aged | DNA Mismatch Repair - genetics | Mass Screening - methods | DNA-Binding Proteins - deficiency | Neoplasm Grading | Endometrial Neoplasms - genetics | DNA Mutational Analysis | MutS Homolog 2 Protein - deficiency | Nuclear Proteins - deficiency | Aged, 80 and over | Adult | Female | Mismatch Repair Endonuclease PMS2 | DNA Repair Enzymes - deficiency | Adenosine Triphosphatases - deficiency | Endometrial Neoplasms - chemistry | Risk Assessment | Colorectal Neoplasms, Hereditary Nonpolyposis - genetics | Risk Factors | California | Biopsy | Adaptor Proteins, Signal Transducing - deficiency | Endometrial Neoplasms - pathology | Aged | Biomarkers, Tumor - genetics | Colorectal Neoplasms, Hereditary Nonpolyposis - chemistry | Index Medicus
Journal Article
Journal of Clinical Oncology, ISSN 0732-183X, 12/2015, Volume 33, Issue 36, pp. 4301 - 4308
Journal Article
American Journal of Surgical Pathology, ISSN 0147-5185, 03/2005, Volume 29, Issue 3, pp. 281 - 294
Journal Article
Journal Article
Journal of the National Cancer Institute, ISSN 0027-8874, 2013, Volume 105, Issue 15, pp. 1142 - 1150
Journal Article
Journal Article