Terminal deletion of 6p results in a recognizable phenotype

American Journal of Medical Genetics

Volumn 136 A, Issue 2, 2005, Pages 162-168

  Lin, Ruth J ^a   Cherry, Athena M ^a   Chen, Kelly C ^a   Lyons, Michael ^a   Hoyme, H Eugene ^a   Hudgins, Louanne ^a  

^a STANFORD UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

Chromosome 6p deletion; Dandy Walker malformation; Developmental delay; Eye abnormalities

Indexed keywords

ANTERIOR EYE CHAMBER DISEASE; ARTICLE; CASE REPORT; CHROMOSOME 6P; CHROMOSOME ANALYSIS; CHROMOSOME DELETION; CONGENITAL HEART MALFORMATION; CONGENITAL MALFORMATION; CYTOGENETICS; DANDY WALKER SYNDROME; DEVELOPMENTAL DISORDER; FEMALE; HEARING LOSS; HUMAN; HYPERTELORISM; NEWBORN; PALPEBRAL FISSURE ANOMALY; PHENOTYPE; PRIORITY JOURNAL;

ABNORMALITIES, MULTIPLE; CHILD, PRESCHOOL; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 6; DANDY-WALKER SYNDROME; DEVELOPMENTAL DISABILITIES; EYE ABNORMALITIES; FEMALE; HEART DEFECTS, CONGENITAL; HUMANS; HYPERTELORISM; INFANT; NOSE; PHENOTYPE;

EID: 22044447468     PISSN: 15524825     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.a.30784     Document Type: Article

References (22)

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