Identification and characterization of CFTR gene mutations in Indian CF patients

Annals of Human Genetics

Volumn 73, Issue 1, 2009, Pages 26-33

  Sharma, N ^a   Singh, M ^a   Kaur, G ^b   Thapa, B R ^a   Prasad, Rajendra ^a  

^a POSTGRADUATE INSTITUTE OF MEDICAL EDUCATION AND RESEARCH   (India)

^b GOVERNMENT MEDICAL COLLEGE AND HOSPITAL   (India)

Author keywords

ARMSPCR; CFTR; Cystic fibrosis; Delta F508; Haplotype; SSCP

Indexed keywords

TRANSMEMBRANE CONDUCTANCE REGULATOR;

ALLELE; ARTICLE; CLINICAL ARTICLE; CYSTIC FIBROSIS; DEMOGRAPHY; EXON; FAMILY HISTORY; FEMALE; GENE DELETION; GENE MUTATION; GENETIC ANALYSIS; GENETIC ASSOCIATION; GENETIC LINKAGE; GENETIC MARKER; HAPLOTYPE; HUMAN; INDIAN; INFANT; MALE; PREDICTION; PRESCHOOL CHILD; PRIORITY JOURNAL; PROMOTER REGION;

CASE-CONTROL STUDIES; CHILD; CHILD, PRESCHOOL; CYSTIC FIBROSIS; CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR; FEMALE; HAPLOTYPES; HUMANS; INDIA; INFANT; MALE; MUTATION;

EID: 58149305457     PISSN: 00034800     EISSN: 14691809     Source Type: Journal    
DOI: 10.1111/j.1469-1809.2008.00477.x     Document Type: Article

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