Identification of the origin of centromeres in whole-arm translocations using fluorescent in situ hybridization with α-satellite DNA probes

American Journal of Medical Genetics

Volumn 40, Issue 1, 1991, Pages 117-120

  Tharapel, A T ^a   Qumsiyeh, M B ^a   Martens, P R ^a   Tharapel, S A ^a   Dalton, J D ^a   Ward, J C ^a   Wilroy Jr , R S ^a  

^a UNIVERSITY OF TENNESSEE HEALTH SCIENCE CENTER   (United States)

Author keywords

monosomy 18p; nonradioactive in situ hybridization; trisomy 18q; whole arm translocation; satellite DNA

Indexed keywords

SATELLITE DNA;

ARTICLE; CASE REPORT; CENTROMERE; CHROMOSOME ANALYSIS; CHROMOSOME TRANSLOCATION 18; DNA PROBE; FEMALE; FLUORESCENCE MICROSCOPY; HUMAN; HUMAN CELL; IN SITU HYBRIDIZATION; INFANT; MENTAL RETARDATION MALFORMATION SYNDROME; PRIORITY JOURNAL;

EID: 0025871352     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.1320400125     Document Type: Article

References (0)