Partial hexasomy 15pter-->15q13 including SNRPN and D15S10: first molecular cytogenetically proven case report.

Journal of medical genetics

Volumn 40, Issue 3, 2003, Pages

  Nietzel, A ^a   Albrecht, B ^a   Starke, H ^a   Heller, A ^a   Gillessen Kaesbach, G ^a   Claussen, U ^a   Liehr, T ^a  

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

AUTOANTIGEN; MICROSATELLITE DNA; SM NUCLEAR ANTIGENS; SMALL NUCLEAR RIBONUCLEOPROTEIN;

ANEUPLOIDY; CASE REPORT; CHROMOSOME 15; CONGENITAL HEART MALFORMATION; DEVELOPMENTAL DISORDER; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENETICS; HEMANGIOMA; HUMAN; KARYOTYPING; LETTER; MICROCEPHALY; MULTIPLE MALFORMATION SYNDROME; MUSCULAR DYSTROPHY; PATHOLOGY; POLYDACTYLY; PRESCHOOL CHILD;

ABNORMALITIES, MULTIPLE; ANEUPLOIDY; AUTOANTIGENS; CHILD, PRESCHOOL; CHROMOSOMES, HUMAN, PAIR 15; DEVELOPMENTAL DISABILITIES; FEMALE; HEART DEFECTS, CONGENITAL; HEMANGIOMA; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; KARYOTYPING; MICROCEPHALY; MICROSATELLITE REPEATS; MUSCULAR DYSTROPHIES; POLYDACTYLY; RIBONUCLEOPROTEINS, SMALL NUCLEAR;

EID: 18844468257     PISSN: None     EISSN: 14686244     Source Type: Journal    
DOI: 10.1136/jmg.40.3.e28     Document Type: Letter

References (0)