Chromosome 22q11 microdeletion in conotruncal heart defects: clinical presentation, parental origin and de novo mutations.

International journal of molecular medicine

Volumn 7, Issue 5, 2001, Pages 501-505

  Chung, M Y ^a   Lu, J H ^a   Chien, H P ^a   Hwang, B ^a  

^a TAIPEI VETERANS GENERAL HOSPITAL   (Taiwan)

Author keywords

[No Author keywords available]

Indexed keywords

DNA; MICROSATELLITE DNA;

ADOLESCENT; ARTICLE; CHILD; CHROMOSOME 22; CHROMOSOME BANDING PATTERN; CHROMOSOME DELETION; CONGENITAL HEART MALFORMATION; FAMILY HEALTH; FEMALE; GENETICS; GENOTYPE; HUMAN; INFANT; MALE; MUTATION; PATHOLOGY; PRESCHOOL CHILD;

ADOLESCENT; CHILD; CHILD, PRESCHOOL; CHROMOSOME BANDING; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 22; DNA; FAMILY HEALTH; FEMALE; GENOTYPE; HEART DEFECTS, CONGENITAL; HUMANS; INFANT; MALE; MICROSATELLITE REPEATS; MUTATION;

MLCS; MLOWN;

EID: 0035344660     PISSN: 11073756     EISSN: None     Source Type: Journal    
DOI: 10.3892/ijmm.7.5.501     Document Type: Article

References (0)