Analysis of five CFTR mutations in Hungarian cystic fibrosis patients

Journal of Inherited Metabolic Disease

Volumn 19, Issue 3, 1996, Pages 378-

  Nemeth K ^a   Fekete, Gy ^a   Kiss, E ^a   Varadi A ^b   Holics, K ^c   Ujhelyi R ^c  

^a SEMMELWEIS UNIVERSITY OF MEDICINE   (Hungary)

^b INSTITUTE OF EXPERIMENTAL MEDICINE   (Hungary)

^c Children's Hospital Heim Pál ^*  (Hungary)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; AMNION CELL; ARTICLE; CHILD; CHORION VILLUS; CHROMOSOME; CYSTIC FIBROSIS; GENE FREQUENCY; GENE MUTATION; GENETIC ANALYSIS; HUMAN; HUNGARY; INFANT; MAJOR CLINICAL STUDY; POINT MUTATION; POLYMERASE CHAIN REACTION; PRENATAL DIAGNOSIS;

ADOLESCENT; ADULT; CHILD; CHILD, PRESCHOOL; CYSTIC FIBROSIS; CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR; HUMANS; INFANT; MUTATION;

EID: 0029946948     PISSN: 01418955     EISSN: None     Source Type: Journal    
DOI: 10.1007/BF01799276     Document Type: Article

References (2)

1. Kogan SC, SC, Gitschier J (1990) Genetic prediction of hemophilia A. In Innis MA, Gelfand DH, Sninsky JJ, White TJ, eds. PCR Protocols. San Diego: Academic Press, 288-299.
2. Schwartz EI, Khalchitsky SE, Eisensmith RC, Woo SLC (1990) Polymerase chain reaction amplification from dried blood spots on Guthrie cards. Lancet ii: 639-642.