Screening the SLC26A4 gene in probands with deafness and goiter (Pendred syndrome) ascertained from a large group of students of the schools for the deaf in Turkey

Clinical Genetics

Volumn 64, Issue 4, 2003, Pages 371-374

  Tekin, Mustafa ^a   Akcayoz D ^a   Comak E ^a   Bogoclu G ^a   Duman, T ^a   Fitoz, S ^a   Ilhan, I ^a   Akar, N ^a  

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

MITOCHONDRIAL DNA; PENDRIN;

ADOLESCENT; BLOOD SAMPLING; CLINICAL ARTICLE; CONTROLLED STUDY; DNA EXTRACTION; EXON; FAMILY; FEMALE; GENE MUTATION; GENETIC SCREENING; GOITER; HEARING IMPAIRMENT; HOMOZYGOSITY; HUMAN; INTRON; LETTER; MALE; MICROSATELLITE MARKER; MUTATIONAL ANALYSIS; NUCLEIC ACID BASE SUBSTITUTION; PENDRED SYNDROME; PHENOTYPE; PHYSICAL EXAMINATION; POLYACRYLAMIDE GEL ELECTROPHORESIS; POLYMERASE CHAIN REACTION; PREVALENCE; PRIORITY JOURNAL; QUESTIONNAIRE; SCHOOL CHILD; SENSITIVITY AND SPECIFICITY; SIBLING; SINGLE STRAND CONFORMATION POLYMORPHISM; STUDENT; TURKEY (REPUBLIC);

BASE SEQUENCE; CARRIER PROTEINS; CONNEXINS; EAR, INNER; ELECTROPHORESIS, POLYACRYLAMIDE GEL; FEMALE; GENETIC SCREENING; HEARING LOSS, SENSORINEURAL; HUMANS; HYPOTHYROIDISM; MALE; MEMBRANE TRANSPORT PROTEINS; MICROSATELLITE REPEATS; MUTATION; PEDIGREE; SEQUENCE ANALYSIS, DNA; SYNDROME; TOMOGRAPHY, X-RAY COMPUTED; TURKEY;

EID: 0141990470     PISSN: 00099163     EISSN: None     Source Type: Journal    
DOI: 10.1034/j.1399-0004.2003.00144.x     Document Type: Letter

References (18)

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