O43: Characterization of the prenatal renal phenotype associated with 17q12/HNF1B microdeletions
| Main Authors: | , , , , , , , , , , , , , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
Elsevier
2023-01-01
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| Series: | Genetics in Medicine Open |
| Online Access: | http://www.sciencedirect.com/science/article/pii/S2949774423006507 |
| _version_ | 1797341970396348416 |
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| author | 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 |
| author_facet | 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 |
| author_sort | Courtney Verscaj |
| collection | DOAJ |
| first_indexed | 2024-03-08T10:26:40Z |
| format | Article |
| id | doaj.art-7f60b552831447d693790d4f469fbeb8 |
| institution | Directory Open Access Journal |
| issn | 2949-7744 |
| language | English |
| last_indexed | 2024-03-08T10:26:40Z |
| publishDate | 2023-01-01 |
| publisher | Elsevier |
| record_format | Article |
| series | Genetics in Medicine Open |
| spelling | doaj.art-7f60b552831447d693790d4f469fbeb82024-01-27T07:10:05ZengElsevierGenetics in Medicine Open2949-77442023-01-0111100650O43: Characterization of the prenatal renal phenotype associated with 17q12/HNF1B microdeletionsCourtney Verscaj0Frances Velez-Bartolomei1Ethan Bodle2Katie Chan3Michael Lyons4Willa Thorson5Wen-Hann Tan6John Graham7Angela Peron8Fabiola Quintero-Rivera9Elaine Zackai10Mary Ann Thomas11Cathy Stevens12Margaret Adam13Lynne Bird14Marilyn Jones15Dena Matalon16Division of Medical Genetics, Department of Pediatrics, Stanford University, Stanford, CADivision of Medical Genetics, Department of Pediatrics, Stanford University, Stanford, CADivision of Medical Genetics, Department of Pediatrics, Stanford University, Stanford, CADivision of Medical Genetics, Department of Pediatrics, Stanford University, Stanford, CAGreenwood Genetic Center, North Charleston, SCDepartment of Human Genetics, University of Miami Miller School of Medicine, Miami, FLDivision of Genetics and Genomics, Boston Children's Hospital, Harvard Medical School, Boston, MACedars-Sinai Medical Center, Los Angeles, CAMedical Genetics, ASST Santi Paolo e Carlo, San Paolo Hospital, Milan, ItalyDepartments of Pathology, Laboratory Medicine, and Pediatrics, University of California IrvineDivision of Human Genetics, Department of Pediatrics, Children's Hospital of PhiladelphiaDepartments of Medical Genetics and Pediatrics, University of Calgary, Alberta, CanadaErlanger Children’s Hospital, University of Tennessee, Chattanooga, TNDivision of Genetic Medicine, Department of Pediatrics, University of Washington, Seattle, WADepartment of Pediatrics, University of California San Diego and Rady Children’s HospitalDepartment of Pediatrics, University of California San Diego and Rady Children’s HospitalDivision of Medical Genetics, Department of Pediatrics, Stanford University, Stanford, CAhttp://www.sciencedirect.com/science/article/pii/S2949774423006507 |
| spellingShingle | 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 O43: Characterization of the prenatal renal phenotype associated with 17q12/HNF1B microdeletions Genetics in Medicine Open |
| title | O43: Characterization of the prenatal renal phenotype associated with 17q12/HNF1B microdeletions |
| title_full | O43: Characterization of the prenatal renal phenotype associated with 17q12/HNF1B microdeletions |
| title_fullStr | O43: Characterization of the prenatal renal phenotype associated with 17q12/HNF1B microdeletions |
| title_full_unstemmed | O43: Characterization of the prenatal renal phenotype associated with 17q12/HNF1B microdeletions |
| title_short | O43: Characterization of the prenatal renal phenotype associated with 17q12/HNF1B microdeletions |
| title_sort | o43 characterization of the prenatal renal phenotype associated with 17q12 hnf1b microdeletions |
| url | http://www.sciencedirect.com/science/article/pii/S2949774423006507 |
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