An 8-cm interstitial deletion on 4q21-q22 in DNA from an infant with hepatoblastoma overlaps with a commonly deleted region in adult liver cancers

American Journal of Medical Genetics

Volumn 103, Issue 2, 2001, Pages 176-180

  Terada, Yoshie ^a   Imoto, Issei ^b   Nagai, Hisaki ^a   Suwa, Kiyotaka ^c   Momoi, Mariko ^c   Tajiri, Takasi ^a   Onda, Masahiko ^a   Inazawa, Johji ^b   Emi, Mitsuru ^a  

^a NIPPON MEDICAL SCHOOL   (Japan)

^b TOKYO MEDICAL AND DENTAL UNIVERSITY   (Japan)

^c JICHI MEDICAL UNIVERSITY   (Japan)

Author keywords

4q21 q22 syndrome; Chromosome aberration; Fluorescence in situ hybridization; Hepatoblastoma; Hepatocellular carcinoma

Indexed keywords

ALPHA FETOPROTEIN;

ADULT; ALEXANDER DISEASE; ARTICLE; CASE REPORT; CHROMOSOME 4Q; CHROMOSOME ANALYSIS; DISEASE ASSOCIATION; FLUORESCENCE IN SITU HYBRIDIZATION; GENE DELETION; GENETIC ANALYSIS; GENOME; HEART ATRIUM SEPTUM DEFECT; HEART VENTRICLE SEPTUM DEFECT; HEPATOBLASTOMA; HUMAN; LIVER CARCINOMA; LYMPHOBLAST; MALE; MENTAL DEFICIENCY; ONSET AGE; PATENT DUCTUS ARTERIOSUS; PRIORITY JOURNAL; PROMOTER REGION; SEIZURE;

ADULT; CHROMOSOME BANDING; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 4; DNA, NEOPLASM; FATAL OUTCOME; HEPATOBLASTOMA; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT; LIVER NEOPLASMS; MALE; MICROSATELLITE REPEATS;

EID: 0035479061     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.1521     Document Type: Article

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