Detection of a familial cryptic translocation by fluorescent in situ hybridisation [1]

Journal of Medical Genetics

Volumn 33, Issue 1, 1996, Pages 84-

  Smith, D P ^a   Floyd, M ^a   Say, B ^a  

^a HA Chapman Institute of Medical Genetics   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CHROMOSOME TRANSLOCATION; FAMILIAL DISEASE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; IN SITU HYBRIDIZATION; LETTER; PRIORITY JOURNAL;

ABNORMALITIES, MULTIPLE; ADULT; CHILD, PRESCHOOL; CHROMOSOMES, HUMAN, PAIR 17; CHROMOSOMES, HUMAN, PAIR 22; FATAL OUTCOME; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT; MALE; MIDDLE AGED; SYNDROME; TRANSLOCATION, GENETIC;

EID: 0030049543     PISSN: 00222593     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Letter

References (0)