del(6)(q12q15) as the sole cytogenetic anomaly in a case of solitary infantile myofibromatosis.

Oncology reports

Volumn 6, Issue 5, 1999, Pages 1101-1104

  Stenman, G ^a   Nadal, N ^a   Persson, S ^a   Gunterberg, B ^a   Angervall, L ^a  

^a SAHLGRENSKA UNIVERSITY HOSPITAL   (Sweden)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CASE REPORT; CHROMOSOME 6; CHROMOSOME DELETION; GENETICS; HUMAN; KARYOTYPING; LEIOMYOMA; MALE; NEWBORN; PATHOLOGY; PATHOPHYSIOLOGY; PRESCHOOL CHILD; WRIST;

CHILD, PRESCHOOL; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 6; HUMANS; INFANT, NEWBORN; KARYOTYPING; MALE; MYOFIBROMATOSIS; WRIST;

MLCS; MLOWN;

EID: 0033192470     PISSN: 1021335X     EISSN: None     Source Type: Journal    
DOI: 10.3892/or.6.5.1101     Document Type: Article

References (0)