Interstitial deletion of chromosome 9, int del(9)(9q22.31-q31.2), including the genes causing multiple basal cell nevus syndrome and Robinow/brachydactyly 1 syndrome

European Journal of Pediatrics

Volumn 162, Issue 2, 2003, Pages 100-103

  Olivieri, C ^b   Maraschio, P ^b   Caselli, D ^c   Martini, C ^c   Beluffi, G ^c   Maserati, E ^d   Danesino, C ^a,c  

^a Genetica Medica   (Italy)

^b UNIVERSITY OF PAVIA   (Italy)

^c FONDAZIONE IRCCS POLICLINICO SAN MATTEO   (Italy)

^d UNIVERSITY OF INSUBRIA   (Italy)

Author keywords

Chromosome 9; Chromosome deletion; Metacarpophalangeal profile; NBCCS; Robinow syndrome

Indexed keywords

ARTICLE; BASAL CELL; BASAL CELL CARCINOMA; BONE AGE; BRACHYDACTYLY; CASE REPORT; CHILD; CHROMOSOME 9; CHROMOSOME DELETION; CLINICAL FEATURE; CLINICAL TRIAL; CONTROLLED CLINICAL TRIAL; CONTROLLED STUDY; CYTOGENETICS; DISEASE ASSOCIATION; EPICANTHUS; FINGER; GENETIC ANALYSIS; HUMAN; LOW SET EAR; MACROCEPHALY; MALE; METACARPOPHALANGEAL JOINT; MOLECULAR BIOLOGY; MUTATION; NEVUS; PALPEBRAL FISSURE ANOMALY; PHENOTYPE; PRIORITY JOURNAL; ROBINOW SYNDROME;

EID: 12244272138     PISSN: 03406199     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00431-002-1116-4     Document Type: Article

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