Novel association of familial testicular germ cell tumor and autosomal dominant polycystic kidney disease withPKD1mutation

Author:

Truscott Laurel1,Gell Joanna1,Chang Vivian Y.12,Lee Hane34,Strom Samuel P.34,Pillai Rex1,Sisk Anthony1,Martinez-Agosto Julian A.1235,Anderson Martin1,Federman Noah126

Affiliation:

1. Department of Pediatrics; Mattel Children's Hospital at UCLA, David Geffen School of Medicine; University of California; Los Angeles California

2. UCLA Jonsson Comprehensive Cancer Center; University of California; Los Angeles California

3. UCLA Clinical Genomics Center; University of California; Los Angeles California

4. Department of Pathology and Laboratory Medicine, David Geffen School of Medicine; University of California; Los Angeles California

5. Department of Human Genetics, David Geffen School of Medicine; University of California; Los Angeles California

6. Department of Orthopaedics, David Geffen School of Medicine; University of California; Los Angeles California

Funder

David Geffen School of Medicine

UCLA Children's Discovery and Innovation Institute

UCLA Clinical Genomics Center

Jonsson Comprehensive Cancer Center

Publisher

Wiley

Subject

Oncology,Hematology,Pediatrics, Perinatology and Child Health

Reference10 articles.

1. Familial testicular germ cell tumors (FTGCT): Overview of a multidisciplinary etiologic study;Greene;Andrology,2015

2. Familial testicular cancer: lack of evidence for trinucleotide repeat expansions and association with PKD1 in one family;Teh;J Med Genet,1999

3. Loss of heterozygosity on chromosome arms 5q, 11p, 13q, and 16p in human testicular germ cell tumors;Al-Jehani;Genes Chromosomes Cancer,1995

4. Exome Aggregation Consortium, The Broad Institute http://exac.broadinstitute.org

5. The polycystic kidney disease 1 gene encodes a 14 kb transcript and lies within a duplicated region on chromosome 16;The European Polycystic Kidney Disease Consortium;Cell,1994

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