Molecular analysis in Brazilian cystic fibrosis patients reveals five novel mutations

Genetic Testing

Volumn 4, Issue 1, 2000, Pages 69-74

  Bernardino, A L F ^a   Ferri, A ^a   Passos Bueno, M R ^a   Kim, C E A ^a   Nakaie, C M A ^a   Gomes, C E T ^b   Damaceno, N ^c   Zatz, M ^a  

^a UNIVERSITY OF SÃO PAULO   (Brazil)

^b FEDERAL UNIVERSITY OF SÃO PAULO   (Brazil)

^c Unidade de Pediatria   (Brazil)

Author keywords

[No Author keywords available]

Indexed keywords

CHLORIDE; DNA; HETERODUPLEX; TRANSMEMBRANE CONDUCTANCE REGULATOR;

ARTICLE; BRAZIL; CHILD; CHROMOSOME; CYSTIC FIBROSIS; DNA SEQUENCE; EXON; FEMALE; GENE; GENE MUTATION; HETERODUPLEX ANALYSIS; HUMAN; INFANT; INTRON; MAJOR CLINICAL STUDY; MALE; POLYMERASE CHAIN REACTION; PRENATAL DIAGNOSIS; SINGLE STRAND CONFORMATION POLYMORPHISM;

AFRICAN CONTINENTAL ANCESTRY GROUP; ALLELES; BRAZIL; CHROMOSOMES; CONTINENTAL POPULATION GROUPS; CYSTIC FIBROSIS; CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR; DNA MUTATIONAL ANALYSIS; EUROPEAN CONTINENTAL ANCESTRY GROUP; EXONS; FEMALE; GENE FREQUENCY; GENETIC SCREENING; GENOTYPE; HETERODUPLEX ANALYSIS; HUMANS; INTRONS; MALE; MUTATION; POLYMORPHISM, GENETIC; PRENATAL DIAGNOSIS;

EID: 0034090798     PISSN: 10906576     EISSN: None     Source Type: Journal    
DOI: 10.1089/109065700316516     Document Type: Article

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