Characterization of familial partial 10p trisomy by chromosomal microdissection, FISH, and microsatellite dosage analysis

Human Genetics

Volumn 98, Issue 4, 1996, Pages 396-402

  Stone, Deborah ^a   Ning, Yi ^b   Guan, Xin Yuan ^b   Kaiser Kupfer, Muriel ^c   Wynshaw Boris, Anthony ^a   Biesecker, Leslie ^a  

^a NATIONAL HUMAN GENOME RESEARCH INSTITUTE   (United States)

^b NATIONAL INSTITUTES OF HEALTH   (United States)

^c NATIONAL EYE INSTITUTE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME 9; CHROMOSOME MICRODISSECTION; CHROMOSOME PAINTING; CHROMOSOME SATELLITE; CLINICAL ARTICLE; DNA PROBE; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; MALE; METAPHASE; PARTIAL TRISOMY 10; PRIORITY JOURNAL;

ABNORMALITIES, MULTIPLE; ADOLESCENT; BASE SEQUENCE; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 10; CHROMOSOMES, HUMAN, PAIR 9; DNA PRIMERS; DNA, SATELLITE; EYE ABNORMALITIES; FEMALE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; KARYOTYPING; LYMPHOCYTES; MALE; MICROSATELLITE REPEATS; MOLECULAR SEQUENCE DATA; PEDIGREE; TRANSLOCATION, GENETIC; TRISOMY;

EID: 0029814318     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004390050228     Document Type: Article

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