Supernumerary ring chromosome 17 identified by fluorescent in situ hybridization

American Journal of Medical Genetics

Volumn 69, Issue 4, 1997, Pages 352-355

  Fagan, Kerry ^a   Edwards, Matthew ^b  

^a JOHN HUNTER HOSPITAL   (Australia)

^b Hunter Genetics   (Australia)

Author keywords

fluorescence in situ hybridization; ring marker chromosome 17; supernumerary marker chromosomes

Indexed keywords

ARTICLE; CASE REPORT; CHILD; CHROMOSOME 17; CLINICAL FEATURE; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; MALFORMATION SYNDROME; MARKER CHROMOSOME; PRESCHOOL CHILD; PRIORITY JOURNAL; RING CHROMOSOME; SUPERNUMERARY CHROMOSOME;

ABNORMALITIES, MULTIPLE; CHILD, PRESCHOOL; CHROMOSOMES, HUMAN, PAIR 17; FEMALE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; RING CHROMOSOMES;

EID: 0030915282     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19970414)69:4<352::AID-AJMG3>3.0.CO;2-N     Document Type: Article

References (20)

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