Deletions of 20p12 in alagille syndrome: Frequency and molecular characterization

American Journal of Medical Genetics

Volumn 70, Issue 1, 1997, Pages 80-86

  Krantz, Ian D ^a   Rand, Elizabeth B ^a   Genin, Anna ^a   Hunt, Piper ^a   Jones, Marilyn ^b   Louis, Anthonise A ^a   Graham Jr , John M ^c   Bhatt, Sucheta ^c   Piccoli, David A ^a   Spinner, Nancy B ^a  

^a CHILDREN S HOSPITAL OF PHILADELPHIA   (United States)

^b RADY CHILDREN'S HOSPITAL   (United States)

^c UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

20p deletions; Alagille syndrome; bile duct paucity and cardiac disease

Indexed keywords

ALAGILLE SYNDROME; ARTICLE; CASE REPORT; CHOLESTASIS; CHROMOSOME 20P; FACE MALFORMATION; GENE DELETION; HEART DISEASE; HUMAN; PRIORITY JOURNAL; SKELETON MALFORMATION;

ADOLESCENT; ALAGILLE SYNDROME; CHILD; CHILD, PRESCHOOL; CHROMOSOME BANDING; CHROMOSOME DELETION; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 20; FEMALE; GENETIC MARKERS; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT; MALE; PEDIGREE;

EID: 0030890169     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19970502)70:1<80::AID-AJMG15>3.0.CO;2-T     Document Type: Article

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