Additional patient with del(12)(q21.2q22): Further evidence for a candidate region for cardio-facio-cutaneous syndrome?

American Journal of Medical Genetics

Volumn 110, Issue 1, 2002, Pages 51-56

  Rauen, Katherine A ^a,b   Albertson, Donna G ^b   Pinkel, Daniel ^a,c   Cotter, Philip D ^a,d  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b UNIVERSITY OF CALIFORNIA   (United States)

^c UNIVERSITY OF CALIFORNIA   (United States)

^d CHILDREN S HOSPITAL OAKLAND   (United States)

Author keywords

Array CGH; Cardio facio cutaneous syndrome; Chromosome 12; Deletion

Indexed keywords

ARTICLE; BACTERIAL ARTIFICIAL CHROMOSOME; CARDIOFACIOCUTANEOUS SYNDROME; CASE REPORT; CHROMOSOMAL LOCALIZATION; CHROMOSOME 12Q; CHROMOSOME DELETION; COMPARATIVE GENOMIC HYBRIDIZATION; CONGENITAL HEART MALFORMATION; CONGENITAL MALFORMATION; DEVELOPMENTAL DISORDER; ECTODERMAL DYSPLASIA; FACE DYSMORPHIA; FACE MALFORMATION; GENE EXPRESSION; GENE LOCUS; GENE SEQUENCE; HUMAN; HUMAN CELL; KARYOTYPE 47,XXY; LYMPHOCYTE; MALE; PHENOTYPE; PRESCHOOL CHILD; PRIORITY JOURNAL; Y CHROMOSOME;

ABNORMALITIES, MULTIPLE; CHILD, PRESCHOOL; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 12; DEVELOPMENTAL DISABILITIES; FACE; FOLLOW-UP STUDIES; HEART DEFECTS, CONGENITAL; HUMANS; INFANT; INFANT, NEWBORN; KARYOTYPING; MALE; SKIN ABNORMALITIES; SYNDROME;

EID: 0036605189     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.10478     Document Type: Article

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