Campomelic syndrome and deletion of SOX9

American Journal of Medical Genetics

Volumn 84, Issue 1, 1999, Pages 20-24

  Olney, Patricia N ^a   Kean, Leslie S ^a   Graham, David ^a   Elsas, Louis J ^a   May, Kristin M ^a  

^a EMORY UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

Campomelic syndrome; Interstitial deletion chromosome 17; SOX9 gene

Indexed keywords

DNA; TRANSCRIPTION FACTOR;

ARTICLE; CAMPTOMELIC DYSPLASIA; CASE REPORT; CHONDROGENESIS; CHROMOSOME 17Q; CHROMOSOME ANALYSIS; CYTOGENETICS; ECHOGRAPHY; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE; GENE DELETION; GENE MUTATION; HUMAN; INTERSTITIAL CHROMOSOME DELETION; MALFORMATION SYNDROME; NEWBORN; PRENATAL DIAGNOSIS; PRIORITY JOURNAL;

BONE DISEASES, DEVELOPMENTAL; CHONDROGENESIS; CHROMOSOME BREAKAGE; CHROMOSOMES, HUMAN, PAIR 17; FEMALE; FIBROBLASTS; GENE DELETION; HIGH MOBILITY GROUP PROTEINS; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT, NEWBORN; KARYOTYPING; TRANSCRIPTION FACTORS;

EID: 0033531956     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19990507)84:1<20::AID-AJMG5>3.0.CO;2-N     Document Type: Article

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