New insights into the phenotypes of 6q deletions

American Journal of Medical Genetics

Volumn 70, Issue 4, 1997, Pages 377-386

  Hopkin, R J ^a,d   Schorry, E ^a   Bofinger, M ^a   Milatovich, A ^b   Stern, H J ^c   Jayne, C ^a   Saal, H M ^a  

^a CINCINNATI CHILDREN S HOSPITAL RESEARCH FOUNDATION   (United States)

^b STANFORD UNIVERSITY MEDICAL CENTER   (United States)

^c CHILDREN'S NATIONAL MEDICAL CENTER   (United States)

^d CINCINNATI CHILDREN'S HOSPITAL MEDICAL CENTER   (United States)

Author keywords

Cardiac anomaly; Chromosome 6; Deletion; Limb malformation; mMntal retardation; Multiple anomalies; Recognizable phenotype

Indexed keywords

AORTOPULMONARY SEPTAL DEFECT; ARTICLE; CASE REPORT; CHILD; CHROMOSOME 6Q; CONGENITAL HEART MALFORMATION; EAR MALFORMATION; GENE DELETION; GROWTH RETARDATION; HUMAN; LIMB MALFORMATION; MALE; MENTAL DEFICIENCY; MUSCLE HYPOTONIA; PHENOTYPE; PRIORITY JOURNAL; SYNDROME;

ADULT; CHILD, PRESCHOOL; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 6; EAR; FEMALE; GROWTH DISORDERS; HUMANS; KARYOTYPING; MALE; MUSCLE HYPOTONIA; PHENOTYPE;

EID: 0030906366     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19970627)70:4<377::AID-AJMG9>3.0.CO;2-Q     Document Type: Article

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