Genetics in Medicine Open (Jan 2023)
O43: Characterization of the prenatal renal phenotype associated with 17q12/HNF1B microdeletions
- Courtney Verscaj,
- Frances Velez-Bartolomei,
- Ethan Bodle,
- Katie Chan,
- Michael Lyons,
- Willa Thorson,
- Wen-Hann Tan,
- John Graham,
- Angela Peron,
- Fabiola Quintero-Rivera,
- Elaine Zackai,
- Mary Ann Thomas,
- Cathy Stevens,
- Margaret Adam,
- Lynne Bird,
- Marilyn Jones,
- Dena Matalon
Affiliations
- Courtney Verscaj
- Division of Medical Genetics, Department of Pediatrics, Stanford University, Stanford, CA
- Frances Velez-Bartolomei
- Division of Medical Genetics, Department of Pediatrics, Stanford University, Stanford, CA
- Ethan Bodle
- Division of Medical Genetics, Department of Pediatrics, Stanford University, Stanford, CA
- Katie Chan
- Division of Medical Genetics, Department of Pediatrics, Stanford University, Stanford, CA
- Michael Lyons
- Greenwood Genetic Center, North Charleston, SC
- Willa Thorson
- Department of Human Genetics, University of Miami Miller School of Medicine, Miami, FL
- Wen-Hann Tan
- Division of Genetics and Genomics, Boston Children's Hospital, Harvard Medical School, Boston, MA
- John Graham
- Cedars-Sinai Medical Center, Los Angeles, CA
- Angela Peron
- Medical Genetics, ASST Santi Paolo e Carlo, San Paolo Hospital, Milan, Italy
- Fabiola Quintero-Rivera
- Departments of Pathology, Laboratory Medicine, and Pediatrics, University of California Irvine
- Elaine Zackai
- Division of Human Genetics, Department of Pediatrics, Children's Hospital of Philadelphia
- Mary Ann Thomas
- Departments of Medical Genetics and Pediatrics, University of Calgary, Alberta, Canada
- Cathy Stevens
- Erlanger Children’s Hospital, University of Tennessee, Chattanooga, TN
- Margaret Adam
- Division of Genetic Medicine, Department of Pediatrics, University of Washington, Seattle, WA
- Lynne Bird
- Department of Pediatrics, University of California San Diego and Rady Children’s Hospital
- Marilyn Jones
- Department of Pediatrics, University of California San Diego and Rady Children’s Hospital
- Dena Matalon
- Division of Medical Genetics, Department of Pediatrics, Stanford University, Stanford, CA
- Journal volume & issue
-
Vol. 1,
no. 1
p. 100650