Genotype-phenotype correlation in five cystic fibrosis patients homozygous for the 621+1G→T mutation [1]

Journal of Medical Genetics

Volumn 34, Issue 9, 1997, Pages 788-789

  De Braekeleer, M ^a   Allard, C ^a   Leblanc, J P ^a   Simard, F ^a   Aubin, G ^a  

^a UNIVERSITÉ DU QUÉBEC À CHICOUTIMI   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; CLINICAL ARTICLE; CYSTIC FIBROSIS; FEMALE; GENE MUTATION; GENOTYPE; HOMOZYGOSITY; HUMAN; LETTER; MALE; NUCLEIC ACID BASE SUBSTITUTION; PHENOTYPE; PRIORITY JOURNAL; SCHOOL CHILD;

ADOLESCENT; ADULT; CHILD; CYSTIC FIBROSIS; FEMALE; HOMOZYGOTE; HUMANS; MALE; MUTATION; PHENOTYPE;

EID: 0030884019     PISSN: 00222593     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Letter

References (13)