Exome sequencing of child-parent trios with bladder exstrophy: Findings in 26 children.
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| Title: | Exome sequencing of child-parent trios with bladder exstrophy: Findings in 26 children. |
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| Authors: | Pitsava G; Division of Intramural Population Health Research, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland, USA., Feldkamp ML; Division of Medical Genetics, Department of Pediatrics, University of Utah School of Medicine, Salt Lake City, Utah, USA., Pankratz N; Department of Laboratory Medicine and Pathology, University of Minnesota Medical School, Minneapolis, Minnesota, USA., Lane J; Department of Laboratory Medicine and Pathology, University of Minnesota Medical School, Minneapolis, Minnesota, USA., Kay DM; Division of Genetics, Wadsworth Center, New York State Department of Health, Albany, New York, USA., Conway KM; Department of Epidemiology, College of Public Health, The University of Iowa, Iowa City, Iowa, USA., Shaw GM; Department of Pediatrics, Stanford University School of Medicine, Stanford, California, USA., Reefhuis J; National Center on Birth Defects and Developmental Disabilities, Centers for Disease Control and Prevention, Atlanta, Georgia, USA., Jenkins MM; National Center on Birth Defects and Developmental Disabilities, Centers for Disease Control and Prevention, Atlanta, Georgia, USA., Almli LM; National Center on Birth Defects and Developmental Disabilities, Centers for Disease Control and Prevention, Atlanta, Georgia, USA., Olshan AF; Department of Epidemiology, Gillings School of Global Public Health, Chapel Hill, North Carolina, USA., Pangilinan F; Gene and Environment Interaction Section, National Human Genome Research Institute, Bethesda, Maryland, USA., Brody LC; Gene and Environment Interaction Section, National Human Genome Research Institute, Bethesda, Maryland, USA., Sicko RJ; Division of Genetics, Wadsworth Center, New York State Department of Health, Albany, New York, USA., Hobbs CA; Rady Children's Institute for Genomic Medicine, San Diego, California, USA., Bamshad M; Department of Pediatrics, University of Washington, Seattle, Washington, USA., McGoldrick D; Department of Genome Sciences, University of Washington, Seattle, Washington, USA., Nickerson DA; Department of Genome Sciences, University of Washington, Seattle, Washington, USA., Finnell RH; Center for Precision Environmental Health, Baylor College of Medicine, Houston, Texas, USA., Mullikin J; National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, USA., Romitti PA; Department of Epidemiology, College of Public Health, The University of Iowa, Iowa City, Iowa, USA., Mills JL; Division of Intramural Population Health Research, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland, USA. |
| Corporate Authors: | University of Washington Center for Mendelian Genomics, NISC Comparative Sequencing Program and the National Birth Defects Prevention Study |
| Source: | American journal of medical genetics. Part A [Am J Med Genet A] 2021 Oct; Vol. 185 (10), pp. 3028-3041. Date of Electronic Publication: 2021 Aug 05. |
| Publication Type: | Journal Article; Research Support, N.I.H., Extramural; Research Support, N.I.H., Intramural; Research Support, U.S. Gov't, P.H.S. |
| Journal Info: | Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 101235741 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1552-4833 (Electronic) Linking ISSN: 15524825 NLM ISO Abbreviation: Am J Med Genet A Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
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| ISSN: | 1552-4833 |
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| DOI: | 10.1002/ajmg.a.62439 |
