Unusual de novo t(13;15)(q12.1;p13) translocation leading to complex mosaicism including jumping translocation

Annales de Genetique

Volumn 41, Issue 1, 1998, Pages 22-26

  Petit, P ^a   Devriendt, K ^a   Vermeesch, J R ^a   De Cock, P ^a   Fryns, J P ^a  

^a UNIVERSITY HOSPITALS LEUVEN   (Belgium)

Author keywords

Cataract; del(13)(pter q12.1); FISH; Jumping translocation; Mosaicism; Neurosensory deafness; Robertsonian translocation

Indexed keywords

ACROCENTRIC CHROMOSOME; ADULT; ARTICLE; CASE REPORT; CATARACT; CELL LINE; CHROMOSOME BANDING PATTERN; CHROMOSOME BREAKAGE; CHROMOSOME MOSAICISM; CHROMOSOME TRANSLOCATION 13; CHROMOSOME TRANSLOCATION 15; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; HUMAN CELL; KARYOTYPE; MALE; MENTAL DEFICIENCY; PERCEPTION DEAFNESS; ROBERTSONIAN CHROMOSOME TRANSLOCATION; TELOMERE;

ROBERTSONIA;

EID: 0031923651     PISSN: 00033995     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (21)