Campomelic dysplasia translocation breakpoints are scattered over 1 Mb proximal to SOX9: Evidence for an extended control region

American Journal of Human Genetics

Volumn 65, Issue 1, 1999, Pages 111-124

  Pfeifer, Dietmar ^a   Kist, Ralf ^a   Dewar, Ken ^b   Devon, Keri ^b   Lander, Eric S ^b   Birren, Bruce ^b   Korniszewski, Lech ^c   Back, Elke ^a   Scherer, Gerd ^a  

^a UNIVERSITY OF FREIBURG   (Germany)

^b WHITEHEAD INSTITUTE FOR BIOMEDICAL RESEARCH   (United States)

^c MEDICAL UNIVERSITY OF WARSAW   (Poland)

Author keywords

[No Author keywords available]

Indexed keywords

ANIMAL CELL; ARTICLE; BONE DYSPLASIA; CASE REPORT; CHROMOSOME 17Q; CHROMOSOME REARRANGEMENT; CHROMOSOME TRANSLOCATION; CONTROLLED STUDY; DNA FLANKING REGION; DNA LIBRARY; EXON; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE CONTROL; GENE MUTATION; GENOME; HUMAN; HUMAN CELL; HYBRID CELL; MALE; MOUSE; NEWBORN; NONHUMAN; NORTHERN BLOTTING; NUCLEOTIDE SEQUENCE; OPEN READING FRAME; PRIORITY JOURNAL; RESTRICTION MAPPING; SEQUENCE TAGGED SITE; YEAST ARTIFICIAL CHROMOSOME;

ANIMALIA; BACTERIA (MICROORGANISMS);

EID: 0033358653     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/302455     Document Type: Article

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