Compound and double mutations in patients with hypertrophic cardiomyopathy: implications for genetic testing and counselling.

Journal of medical genetics

Volumn 42, Issue 10, 2005, Pages

  Ingles, J ^a   Doolan, A ^a   Chiu, C ^a   Seidman, J ^a   Seidman, C ^a   Semsarian, C ^a  

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; AGED; COHORT ANALYSIS; DIAGNOSTIC PROCEDURE; DNA SEQUENCE; FEMALE; GENETIC COUNSELING; GENETIC PREDISPOSITION; GENETICS; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; HUMAN; HYPERTROPHIC CARDIOMYOPATHY; LETTER; MALE; MIDDLE AGED; MUTATION; PEDIGREE; PHENOTYPE;

ADOLESCENT; ADULT; AGED; AGED, 80 AND OVER; CARDIOMYOPATHY, HYPERTROPHIC; CHROMATOGRAPHY, HIGH PRESSURE LIQUID; COHORT STUDIES; FEMALE; GENETIC COUNSELING; GENETIC PREDISPOSITION TO DISEASE; HUMANS; MALE; MIDDLE AGED; MOLECULAR DIAGNOSTIC TECHNIQUES; MUTATION; PEDIGREE; PHENOTYPE; SEQUENCE ANALYSIS, DNA;

EID: 33646757738     PISSN: None     EISSN: 14686244     Source Type: Journal    
DOI: 10.1136/jmg.2005.033886     Document Type: Letter

References (0)