Total is more than the sum of the parts: Phenotyping the heart in cardiovascular genetics clinics

American Journal of Medical Genetics

Volumn 131 A, Issue 2, 2004, Pages 111-114

  Lin, Angela E ^a   Salbert, Bonnie Anne ^b   Belmont, John ^c   Smoot, Leslie ^d  

^a MASSACHUSETTS GENERAL HOSPITAL   (United States)

^b UNIVERSITY OF ROCHESTER MEDICAL CENTER   (United States)

^c BAYLOR COLLEGE OF MEDICINE   (United States)

^d BOSTON CHILDREN S HOSPITAL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AGE; ALAGILLE SYNDROME; AORTA SUPRAVALVULAR STENOSIS; CARDIOVASCULAR MALFORMATION; CHROMOSOME 11P; CHROMOSOME DELETION; CLINICAL GENETICS; CONGENITAL HEART MALFORMATION; COSTELLO SYNDROME; DEXTROCARDIA; DIAPHRAGM HERNIA; FALLOT TETRALOGY; GENETIC COUNSELING; HEART ATRIUM SEPTUM DEFECT; HEART RIGHT VENTRICLE DOUBLE OUTLET; HEART VENTRICLE SEPTUM DEFECT; HUMAN; HYPERTROPHIC CARDIOMYOPATHY; HYPOPLASTIC LEFT HEART SYNDROME; LUNG ATRESIA; MOLECULAR GENETICS; NOONAN SYNDROME; NOTE; PATENT DUCTUS ARTERIOSUS; PATTERN RECOGNITION; PHENOTYPE; PRIORITY JOURNAL; PROGNOSIS; RITSCHER SCHINZEL SYNDROME; SITUS INVERSUS; SMITH LEMLI OPITZ SYNDROME; SUPRAVENTRICULAR TACHYCARDIA; SYMPTOM; SYNDROME; TRISOMY 18; TRISOMY 21; TURNER SYNDROME; VALVULAR HEART DISEASE; WILLIAMS BEUREN SYNDROME;

ACADEMIC MEDICAL CENTERS; CARDIOLOGY; CARDIOVASCULAR ABNORMALITIES; CARDIOVASCULAR DISEASES; GENETICS, MEDICAL; HUMANS; PHENOTYPE; SYNDROME;

EID: 9644283253     PISSN: 15524825     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.a.30304     Document Type: Note

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