Deletion mapping on chromosome 10p and definition of a critical region for the second DiGeorge syndrome locus (DGS2)

European Journal of Human Genetics

Volumn 6, Issue 3, 1998, Pages 213-225

  Schuffenhauer, Simone ^a,j   Lichtner, Peter ^a   Peykar Derakhshandeh, Popak ^a   Murken, Jan ^a   Haas, Oskar A ^b   Back, Elke ^c   Wolff, Gerhard ^c   Zabel, Bernhard ^d   Barisic, Ingeborg ^e   Rauch, Anita ^f   Borochowitz, Zvi ^g   Dallapiccola, Bruno ^h   Ross, Mark ⁱ   Meitinger, Thomas ^a  

^a UNIVERSITY OF MUNICH   (Germany)

^b ST ANNA CHILDREN S HOSPITAL   (Austria)

^c UNIVERSITY OF FREIBURG   (Germany)

^d JOHANNES GUTENBERG UNIVERSITY   (Germany)

^e Children's University Hospital Zagreb   (Croatia)

^f UNIVERSITY OF ERLANGEN NUREMBERG   (Germany)

^g TECHNION ISRAEL INSTITUTE OF TECHNOLOGY   (Israel)

^h UNIVERSITY OF ROME TOR VERGATA   (Italy)

ⁱ WELLCOME TRUST SANGER INSTITUTE   (United Kingdom)

^j LUDWIG MAXIMILIANS UNIVERSITY   (Germany)

more..

Author keywords

Chromosome 10p; Deletion mapping; DGS2; DiGeorge syndrome; Hearing loss; Ptosis

Indexed keywords

ARTICLE; CHROMOSOME 10P; CLINICAL ARTICLE; DIGEORGE SYNDROME; FLUORESCENCE IN SITU HYBRIDIZATION; GENE DELETION; GENE LOCUS; GENE MAPPING; GENE TRANSLOCATION; HUMAN; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; RECIPROCAL CHROMOSOME TRANSLOCATION;

EID: 13144252168     PISSN: 10184813     EISSN: None     Source Type: Journal    
DOI: 10.1038/sj.ejhg.5200183     Document Type: Article

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