Evaluation of newborn screening bloodspot-based genetic testing as second tier screen for bedside newborn hearing screening

Genetics in Medicine

Volumn 13, Issue 12, 2011, Pages 1006-1010

  Schimmenti, Lisa A ^a,c   Warman, Berta ^a,b   Schleiss, Mark R ^a   Daly, Kathleen A ^a   Ross, Julie A ^a   McCann, Mark ^b   Jurek, Anne M ^a   Berry, Susan A ^a  

^a UNIVERSITY OF MINNESOTA   (United States)

^b MINNESOTA DEPARTMENT OF HEALTH   (United States)

^c UNIVERSITY OF MINNESOTA MEDICAL SCHOOL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CONNEXIN 26;

ALLELE; ARTICLE; AUDITORY SCREENING; CASE CONTROL STUDY; CONTROLLED STUDY; FEMALE; GENE FREQUENCY; GENE MUTATION; GENE SEQUENCE; GENETIC SCREENING; HUMAN; MAJOR CLINICAL STUDY; MALE; MUTATION RATE; NEWBORN; NEWBORN BLOODSPOT GENETIC TESTING; NEWBORN SCREENING;

ALLELES; CASE-CONTROL STUDIES; CONNEXINS; DNA MUTATIONAL ANALYSIS; FOLLOW-UP STUDIES; GENETIC TESTING; GENOTYPE; HEARING; HEARING LOSS; HUMANS; INFANT, NEWBORN; MUTATION; NEONATAL SCREENING; PREVALENCE; TUMOR MARKERS, BIOLOGICAL; UNITED STATES;

EID: 82955245718     PISSN: 10983600     EISSN: 15300366     Source Type: Journal    
DOI: 10.1097/GIM.0b013e318226fc2e     Document Type: Article

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