An 18q- syndrome breakpoint resides between the duplicated serpins SCCA1 and SCCA2 and arises via a cryptic rearrangement with satellite III DNA

Human Molecular Genetics

Volumn 8, Issue 1, 1999, Pages 87-92

  Katz, Samuel G ^e   Schneider, Sandra S ^e   Bartuski, Allison ^e   Trask, Barbara J ^b   Massa, Hillary ^b   Overhauser, Joan ^c   Lalande, Marc ^a   Lansdorp, Peter M ^d   Silverman, Gary A ^e  

^a HOWARD HUGHES MEDICAL INSTITUTE   (United States)

^b UNIVERSITY OF WASHINGTON   (United States)

^c THOMAS JEFFERSON UNIVERSITY   (United States)

^d BRITISH COLUMBIA CANCER AGENCY   (Canada)

^e NONE

Author keywords

[No Author keywords available]

Indexed keywords

DNA; SATELLITE DNA; SERINE PROTEINASE INHIBITOR;

ANIMAL CELL; ARTICLE; CHROMOSOME 18Q; CHROMOSOME DELETION; DNA SEQUENCE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE DUPLICATION; GENE REARRANGEMENT; HUMAN; HUMAN CELL; MENTAL RETARDATION MALFORMATION SYNDROME; MOLECULAR CLONING; NONHUMAN; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; PULSED FIELD GEL ELECTROPHORESIS; SEQUENCE HOMOLOGY; TELOMERE;

ABNORMALITIES, MULTIPLE; ANTIGENS, NEOPLASM; BASE SEQUENCE; CELL LINE; CHROMOSOME BREAKAGE; CHROMOSOME DELETION; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 18; DNA, SATELLITE; GENE REARRANGEMENT; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; MENTAL RETARDATION; MOLECULAR SEQUENCE DATA; REPETITIVE SEQUENCES, NUCLEIC ACID; SERPINS; SYNDROME; TELOMERE;

ANIMALIA;

EID: 0032929028     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/8.1.87     Document Type: Article

References (39)

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