Neonatal screening of hemoglobinopathies and G6PD deficiency in Catalonia (Spain). Molecular study of sickle cell disease associated with alpha thalassemia and G6PD deficiency;Cribado neonatal de hemoglobinopatías y déficit de glucosa-6-fosfato deshidrogenasa (G6PD) en Cataluña. Estudio molecular de la anemia falciforme asociada a alfatalasemia y déficit de G6PD

Medicina Clinica

Volumn 129, Issue 5, 2007, Pages 161-164

  Mañú Pereira, María Del Mar ^a,h   Cabot, Anna ^e   González, Ana Martínez ^a   Navarro, Eulalia Sitjà ^a   Cararach, Vicent ^a   Sabrià, Josep ^b   Boixaderas, Jordi ^c   Teixidor, Roser ^d   Bosch, Albert ^e   Vílchez, M Ángeles López ^f   Ibáñez, Itziar Martín ^f   Carrión, Teresa ^g   Plaja, Pere ^g   Sánchez, Mario ^b   Vives Corrons, José Luis ^a  

^a HOSPITAL CLÍNIC   (Spain)

^b HOSPITAL JOSEP TRUETA   (Spain)

^c HOSPITAL UNIVERSITARI JOAN XXIII   (Spain)

^d Hospital Sant Jaume de Calella   (Spain)

^e HOSPITAL DE MATARÓ   (Spain)

^f HOSPITAL DEL MAR   (Spain)

^g Hospital de Palamos   (Spain)

^h UNIVERSITY OF BARCELONA   (Spain)

Author keywords

Alpha thalassaemia; G6PD deficiency; Hemoglobinopathies; Neonatal screening; Sickle cell disease

Indexed keywords

HEMOGLOBIN S;

ALPHA THALASSEMIA; AMPLIFICATION REFRACTORY MUTATION SYSTEM; ARTICLE; BLOOD EXAMINATION; BLOOD SAMPLING; CONTROLLED STUDY; DISEASE ASSOCIATION; EARLY DIAGNOSIS; FEMALE; FLUORESCENCE ANALYSIS; GENETIC ASSOCIATION; GENETIC HETEROGENEITY; GENETIC RISK; GENETIC SCREENING; GENOTYPE PHENOTYPE CORRELATION; GLUCOSE 6 PHOSPHATE DEHYDROGENASE DEFICIENCY; HEMOGLOBINOPATHY; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; HUMAN; INSTRUMENTATION; MAJOR CLINICAL STUDY; MALE; NEWBORN; NEWBORN SCREENING; PREVALENCE; SICKLE CELL ANEMIA; SPAIN;

EID: 34548575235     PISSN: 00257753     EISSN: 15788989     Source Type: Journal    
DOI: 10.1157/13107791     Document Type: Article

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