Recurrent reciprocal genomic rearrangements of 17q12 are associated with renal disease, diabetes, and epilepsy

American Journal of Human Genetics

Volumn 81, Issue 5, 2007, Pages 1057-1069

  Mefford, Heather C ^a,b   Clauin, Séverine ^e   Sharp, Andrew J ^a   Moller, Rikke S ^g,h   Ullmann, Reinhard ⁱ   Kapur, Raj ^c   Pinkel, Dan ^j   Cooper, Gregory M ^a   Ventura, Mario ^a,k   Ropers, H Hilger ⁱ   Tommerup, Niels ^h   Eichler, Evan E ^a,d   Bellanne Chantelot, Christine ^e,f  

^a UNIVERSITY OF WASHINGTON   (United States)

^b UNIVERSITY OF WASHINGTON SCHOOL OF MEDICINE   (United States)

^c SEATTLE CHILDREN S RESEARCH INSTITUTE   (United States)

^d HOWARD HUGHES MEDICAL INSTITUTE   (United States)

^e ASSISTANCE PUBLIQUE HÔPITAUX DE PARIS   (France)

^f SORBONNE UNIVERSITÉ   (France)

^g DANISH EPILEPSY CENTRE   (Denmark)

^h Wilhelm Johannsen Centre for Functional Genome Research   (Denmark)

ⁱ MAX PLANCK INSTITUTE FOR MOLECULAR GENETICS   (Germany)

^j UNIVERSITY OF CALIFORNIA   (United States)

^k UNIVERSITY OF BARI   (Italy)

more..

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; AUTOPSY; COMPARATIVE GENOMIC HYBRIDIZATION; DEVELOPMENTAL DISORDER; DIABETES MELLITUS; EPILEPSY; FETUS; GENE; GENE DELETION; GENE DUPLICATION; GENE MAPPING; GENE REARRANGEMENT; GENETIC ASSOCIATION; HUMAN; KIDNEY DISEASE; MULTICYSTIC DYSPLASTIC KIDNEY; PHENOTYPE; PRIORITY JOURNAL; TCF2 GENE;

EID: 35348827304     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/522591     Document Type: Article

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