| 1341/1644 | US=47 / Biol/Mol Highsmith WE Jr. Electrophoretic methods for mutation detection and DNA sequencing. In: Coleman WB, Tsongalis GJ. Molecular diagnostics: for the clinical laboratorian. 2ª ed. Totowa: Humana Press, 2006. p. 85-109. ISBN 1-58829-356-4. DIAGNOSTICO MOELCULAR; DETECCAO DE MUTACAO; SEQUENCIAMENTO DE DNA; METODOS ELETROFORETICOS; REACAO DE POLIMERASE EM CADEIA; ELETROFORESE; ELETROFORESE CAPILAR; ANALISE DE DADOS; SOFTWARE |
| 1342/1644 | US=47 / Biol/Mol Broeckel U, Hessner MJ. Single-nucleotide polymorphisms: testing DNA variation for disease association. In: Coleman WB, Tsongalis GJ. Molecular diagnostics: for the clinical laboratorian. 2ª ed. Totowa: Humana Press, 2006. p. 111-20. ISBN 1-58829-356-4. DIAGNOSTICO MOELCULAR; POLIMORFISMOS DE NUCLEOTIDEO UNICO; TESTE DE DNA; DETECCAO DE DOENCA |
| 1343/1644 | US=47 / Biol/Mol Hayes DN, Meyerson M. Microarray approaches to gene expression analysis. In: Coleman WB, Tsongalis GJ. Molecular diagnostics: for the clinical laboratorian. 2ª ed. Totowa: Humana Press, 2006. p. 121-48. ISBN 1-58829-356-4. DIAGNOSTICO MOELCULAR; MICROARRAY; ANALISE DE EXPRESSAO GENICA; PLATAFORMA DE MICROARRAY DE DNA; MATRIZES DE OLIGONUCLEOTIDOS; PROTEOMICOS |
| 1344/1644 | US=47 / Biol/Mol Dobrovic A. Methods for analysis of DNA methylation. In: Coleman WB, Tsongalis GJ. Molecular diagnostics: for the clinical laboratorian. 2ª ed. Totowa: Humana Press, 2006. p. 149-60. ISBN 1-58829-356-4. |
| 1345/1644 | US=47 / Biol/Mol DiGiuseppe JA. Flow cytometry. In: Coleman WB, Tsongalis GJ. Molecular diagnostics: for the clinical laboratorian. 2ª ed. Totowa: Humana Press, 2006. p. 163-72. ISBN 1-58829-356-4. DIAGNOSTICO MOELCULAR; CITOMETRIA DE FLUXO; LINFOMA NAO-HODGKIN; ANALISE IMUNOFENOTIPICA; CONTEUDO DE DNA; ANALISE DE PLOIDIA; ANALISE DE DOENCA RESIDUAL MINIMA; HEMOGLOBINURIA NOTURNA PAROXISTICA |
| 1346/1644 | US=47 / Biol/Mol Keagle MB. Medical cytogenetics. In: Coleman WB, Tsongalis GJ. Molecular diagnostics: for the clinical laboratorian. 2ª ed. Totowa: Humana Press, 2006. p. 173-87. ISBN 1-58829-356-4. DIAGNOSTICO MOELCULAR; CITOGENETICA MEDICA; AVALIACAO CROMOSSOMICA; ANORMALIDADES CROMOSSOMICAS |
| 1347/1644 | US=47 / Biol/Mol Mundle SD, Koska RJ. Fluorescence in situ hybridization. In: Coleman WB, Tsongalis GJ. Molecular diagnostics: for the clinical laboratorian. 2ª ed. Totowa: Humana Press, 2006. p. 189-202. ISBN 1-58829-356-4. DIAGNOSTICO MOLECULAR; HIBRIDIZACAO IN SITU POR FLUORESCENCIA; ANALISE CITOGENETICA |
| 1348/1644 | US=47 / Biol/Mol Hunt J, Davydova L, Cartun RW, Baiulescu M. Immunohistochemistry. In: Coleman WB, Tsongalis GJ. Molecular diagnostics: for the clinical laboratorian. 2ª ed. Totowa: Humana Press, 2006. p. 203-17. ISBN 1-58829-356-4. DIAGNOSTICO MOLECULAR; IMUNOHISTOQUIMICA; ANTICORPOS; TECNICAS IMUNOHISTOQUIMICAS; DIAGNOSTICO TUMORAL |
| 1349/1644 | US=47 / Biol/Mol Bagnell CR Jr. Laser capture microdissection. In: Coleman WB, Tsongalis GJ. Molecular diagnostics: for the clinical laboratorian. 2ª ed. Totowa: Humana Press, 2006. p. 219-24. ISBN 1-58829-356-4. DIAGNOSTICO MOLECULAR; MICRODISSECCAO E CAPTURA A LASER; METODOS; INSTRUMENTACAO |
| 1350/1644 | US=47 / Biol/Mol Sabbath-Solitare M, Baptist SJ, Redondo TC. Framework for quality assurance in molecular diagnostics. In: Coleman WB, Tsongalis GJ. Molecular diagnostics: for the clinical laboratorian. 2ª ed. Totowa: Humana Press, 2006. p. 227-36. ISBN 1-58829-356-4. DIAGNOSTICO MOLECULAR; GARANTIA DE QUALIDADE; QUALIFICACAO DE PESSOAL |
| 1351/1644 | US=47 / Biol/Mol Seaton BL. Verification of molecular assays. In: Coleman WB, Tsongalis GJ. Molecular diagnostics: for the clinical laboratorian. 2ª ed. Totowa: Humana Press, 2006. p. 237-41. ISBN 1-58829-356-4. DIAGNOSTICO MOLECULAR; ENSAIOS MOLECULARES; TESTES MOLECULARES; INTERVALO DE REFERENCIA; SENSIBILIDADE ANALITICA; ESPECIFICIDADE ANALITICA; INTERVALO REPORTAVEL; PRECISAO |
| 1352/1644 | US=47 / Biol/Mol Jakupciak JP, O'Connell CD. Standards and standardization of molecular diagnostics. In: Coleman WB, Tsongalis GJ. Molecular diagnostics: for the clinical laboratorian. 2ª ed. Totowa: Humana Press, 2006. p. 243-6. ISBN 1-58829-356-4. DIAGNOSTICO MOLECULAR; NORMAS; PADRONIZACAO; TRINUCLEOTIDEOS; TECNOLOGIA PARA DETECCAO DE MUTACAO; TP53 |
| 1353/1644 | US=47 / Biol/Mol Ferreira-Gonzalez A, Garrett CT. Laboratory-developed tests in molecular diagnostics. In: Coleman WB, Tsongalis GJ. Molecular diagnostics: for the clinical laboratorian. 2ª ed. Totowa: Humana Press, 2006. p. 247-56. ISBN 1-58829-356-4. DIAGNOSTICO MOLECULAR; TESTES DE LABORATORIO; TESTES CLINICOS |
| 1354/1644 | US=47 / Biol/Mol Weidenhammer E, Tsongalis GJ. An overview of molecular genetics. In: Coleman WB, Tsongalis GJ. Molecular diagnostics: for the clinical laboratorian. 2ª ed. Totowa: Humana Press, 2006. p. 259-66. ISBN 1-58829-356-4. DIAGNOSTICO MOLECULAR; GENETICA MOLECULAR; GENOMA HUMANO; DISTURBIOS GENETICOS; VARIACAO DE SEQUENCIA DE DNA; MUTACAO; POLIMORFISMO; PADROES DE HERANCA MENDELIANA; TESTES DE DIAGNOSTICO MOLECULAR |
| 1355/1644 | US=47 / Biol/Mol Nagan N, Klein CJ, Dawson DB, Wick MJ, Thibodeau SN. Genetic basis of neurologic and neuromuscular diseases. In: Coleman WB, Tsongalis GJ. Molecular diagnostics: for the clinical laboratorian. 2ª ed. Totowa: Humana Press, 2006. p. 267-80. ISBN 1-58829-356-4. DIAGNOSTICO MOLECULAR; DOENCAS NEUROLOGICAS; DOENCAS NEUROMUSCULARES; BASES GENETICAS; DISTURBIOS REPETICAO DE TRINUCLEOTIDEOS; ATROFIA MUSCULAR ESPINAL; NEUROFIBROMATOSE TIPO 1; ATAXIA TELANGIECTASIA; NEUROPATIA MOTORA HEREDITARIA; NEUROPATIA SENSORIAL HEREDITARIA; DISTROFIA MUSCULAR DE DUCHENNE |
| 1356/1644 | US=47 / Biol/Mol Potter A, Phillips III JA. Molecular mechanisms of endocrine disorders. In: Coleman WB, Tsongalis GJ. Molecular diagnostics: for the clinical laboratorian. 2ª ed. Totowa: Humana Press, 2006. p. 281-94. ISBN 1-58829-356-4. DIAGNOSTICO MOLECULAR; MECANISMOS MOLECULARES; DOENCAS ENDOCRINAS; MUTACAO; GENETICA MOLECULAR; ENDOCRINOLOGIA; DISTURBIOS DA TIREOIDE; DISTURBIOS DA PARATIREOIDE; ENDOCRINOLOGIA MOLECULAR DA DIABETES MELLITUS |
| 1357/1644 | US=47 / Biol/Mol Wu AHB. Molecular pathogenesis of cardiovascular disease. In: Coleman WB, Tsongalis GJ. Molecular diagnostics: for the clinical laboratorian. 2ª ed. Totowa: Humana Press, 2006. p. 295-309. ISBN 1-58829-356-4. DIAGNOSTICO MOLECULAR; DOENCA CARDIOVASCULAR; PATOGENESE MOLECULAR; GENES TROMBOTICOS; FUNCAO TROMBOLITICA; GLICOPROTEINAS PLAQUETARIAS; FATORES BIOQUIMICOS; OXIDASE NADH/NADPH; MARCADORES PARA INSUFICIENCIA CARDIACA |
| 1358/1644 | US=47 / Clín/Medica Cilloni D, Messa E, Messa F, Carturan S, Defilippi I, Arruga F, Rosso V, Catalano R, Bracco E, Nicoli P, Saglio G. Genetics abnormalities as targets for molecular therapies in myelodysplastic syndromes. In: Bradlow KL, Carruba G. Estrogens and human diseases. Boston: Blackwell, 2006. p. 411-23. ISBN 978-1-57331-699-5. DEFEITOS GENETICOS; SINDROMES MIELODISPLASICAS; TERAPIA MOLECULAR; WT1; EV11; TIROSINA CINASE |
| 1359/1644 | US=47 / Biol/Mol Ballesteros E. Molecular diagnostics in coagulation. In: Coleman WB, Tsongalis GJ. Molecular diagnostics: for the clinical laboratorian. 2ª ed. Totowa: Humana Press, 2006. p. 311-20. ISBN 1-58829-356-4. DIAGNOSTICO MOLECULAR; COAGULACAO; TESTES MOLECULARES DE COAGULACAO; LABORATORIO DE COAGULACAO |
| 1360/1644 | US=47 / Biol/Mol Lewis III EH, Lewis MJ, Amos JA, Tsongalis GJ. Cystic fibrosis. In: Coleman WB, Tsongalis GJ. Molecular diagnostics: for the clinical laboratorian. 2ª ed. Totowa: Humana Press, 2006. p. 321-7. ISBN 1-58829-356-4. DIAGNOSTICO MOLECULAR; FIBROSE CISTICA; GENETICA; TESTES CLINICOS; FIBROSE CISTICA. PATOFISIOLOGIA; FIBROSE CISTICA. ANATOMIA PATOLOGICA |