Complex phenotypes in the haemoglobinopathies: recommendations on screening and DNA testing.

Trent, Ronald J; Webster, Boyd; Bowden, Donald K; Gilbert, Anne; Holl, P Joy; Lindeman, Robert; Lammi, Ahti; Rowell, John; Hinchcliffe, Marcus; Colley, Alison; Wilson, Meredith; Saleh, Mona; Blackwell, Jennifer; Petrou, Vicki

Trent, Ronald J; Webster, Boyd; Bowden, Donald K; Gilbert, Anne; Holl, P Joy; Lindeman, Robert; Lammi, Ahti; Rowell, John; Hinchcliffe, Marcus; Colley, Alison; Wilson, Meredith; Saleh, Mona; Blackwell, Jennifer; Petrou, Vicki.

Afiliação

Trent RJ; Department of Molecular and Clinical Genetics, Royal Prince Alfred Hospital in the Central Clinical School, University of Sydney, New South Wales, Australia. rtrent@med.usyd.edu.au

Pathology ; 38(6): 507-19, 2006 Dec.

Article em En | MEDLINE | ID: mdl-17393977

ABSTRACT

ABSTRACT

This document considers a number of scenarios involving complex haemoglobinopathies and provides 28 recommendations at both the clinical and laboratory levels on how these should be managed.

Assuntos

DNA/genética; Testes Genéticos/métodos; Hemoglobinopatias/diagnóstico; Hemoglobinopatias/genética; DNA/análise; Feminino; Triagem de Portadores Genéticos/métodos; Hemoglobina Falciforme/genética; Humanos; Masculino; Linhagem; Talassemia/genética

Buscar no Google

Imprimir

XML

PubMed Links

Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: DNA / Testes Genéticos / Hemoglobinopatias Tipo de estudo: Diagnostic_studies / Guideline / Prognostic_studies / Screening_studies Limite: Female / Humans / Male Idioma: En Revista: Pathology Ano de publicação: 2006 Tipo de documento: Article País de afiliação: Austrália

Buscar no Google

Imprimir

XML

PubMed Links