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2014, Molecular and Translational Medicine, ISBN 1461481260
Molecular Diagnostics: 12 Tests That Changed Everything focuses on specific laboratory tests and emphasizes how the availability of these tests has altered how... 
Medicine | Pathology | Emerging infectious diseases | Oncology
Web Resource
09/2013, 2014, Molecular and Translational Medicine, ISBN 9781461481263, 260
This book emphasizes how 12 key molecular laboratory tests have altered the way clinicians treat their patients. Each chapter focuses on a specific test  and... 
Pathology, Molecular | Molecular diagnosis | Pathology | Oncology | Infectious Diseases | Medicine & Public Health
eBook
Clinical Chemistry, ISSN 0009-9147, 03/2010, Volume 56, Issue 3, p. 491
Journal Article
PLoS ONE, ISSN 1932-6203, 11/2012, Volume 7, Issue 11, pp. e49083 - e49083
Fuchs endothelial corneal dystrophy (FECD) is a common, familial disease of the corneal endothelium and is the leading indication for corneal transplantation.... 
PATHOGENESIS | APOPTOSIS | CTG REPEAT | UNFOLDED PROTEIN RESPONSE | MENTAL-RETARDATION | ENDOTHELIAL DYSTROPHY | MULTIDISCIPLINARY SCIENCES | INHERITANCE | PITT-HOPKINS-SYNDROME | MISSENSE MUTATIONS | HAPLOINSUFFICIENCY | Blotting, Southern | Fuchs' Endothelial Dystrophy - genetics | Genetic Predisposition to Disease | Reproducibility of Results | Transcription Factor 4 | Humans | Middle Aged | Molecular Sequence Data | Male | Transcription Factors - genetics | Sequence Analysis, DNA | Case-Control Studies | Genome, Human - genetics | Microsatellite Repeats - genetics | Base Sequence | Alleles | Basic Helix-Loop-Helix Leucine Zipper Transcription Factors - genetics | Aged, 80 and over | Trinucleotide Repeat Expansion - genetics | Female | Aged | Chromosomes, Human, Pair 18 - genetics | Genetic aspects | Single nucleotide polymorphisms | Genes | Analysis | Cornea | Transcription factors | Laboratories | Intellectual disabilities | Pathogenesis | Transplantation | Biochemistry | Single-nucleotide polymorphism | Kinases | Gene sequencing | Proteins | Primers | DNA repeat expansion | Southern blotting | Expansion | Chromosomes | Deoxyribonucleic acid--DNA | Edema | Health risks | Data processing | Patients | Endothelium | White blood cells | Corneal dystrophy | Dystrophy | Genetic testing | Molecular biology | DNA sequencing | Apoptosis | Polymorphism | Index Medicus | Deoxyribonucleic acid | DNA
Journal Article
Journal of the American Society of Nephrology, ISSN 1046-6673, 01/2018, Volume 29, Issue 1, pp. 51 - 56
Fibrillary GN (FGN) is a rare primary glomerular disease. Histologic and histochemical features of FGN overlap with those of other glomerular diseases, and no... 
GLOMERULONEPHRITIS | DIAGNOSIS | AMYLOIDOSIS | UROLOGY & NEPHROLOGY | CLASSIFICATION | IMMUNOTACTOID GLOMERULOPATHY | SHOTGUN-PROTEOMICS | PATHOLOGICAL FEATURES | Index Medicus | renal | fibrillary GN | proteomics | DNAJB9 | Brief Communication | biomarker | immunofluorescence
Journal Article
Journal Article
Clinical Chemistry, ISSN 0009-9147, 08/2008, Volume 54, Issue 8, pp. 1399 - 1399
Journal Article
Journal Article
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