Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Kravets, Elijah J"'
Autor:
Kumar, Akash, Zastrow, Diane B, Kravets, Elijah J, Beleford, Daniah, Ruzhnikov, Maura RZ, Grove, Megan E, Dries, Annika M, Kohler, Jennefer N, Waggott, Daryl M, Yang, Yaping, Huang, Yong, Undiagnosed Diseases Network, Mackenzie, Katherine M, Eng, Christine M, Fisher, Paul G, Ashley, Euan A, Teng, Joyce M, Stevenson, David A, Shieh, Joseph T, Wheeler, Matthew T, Bernstein, Jonathan A
Publikováno v:
American journal of medical genetics. Part A, vol 179, iss 6
Phacomatosis pigmentovascularis (PPV) comprises a family of rare conditions that feature vascular abnormalities and melanocytic lesions that can be solely cutaneous or multisystem in nature. Recently published work has demonstrated that both vascular
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::6c8b4012edace3c047606f77b3578cf3
https://escholarship.org/uc/item/7ww536w6
https://escholarship.org/uc/item/7ww536w6
Autor:
Kumar A; Department of Pediatrics, Stanford School of Medicine, Stanford, California., Zastrow DB; Stanford Center for Undiagnosed Diseases, Stanford University, Stanford, California., Kravets EJ; Department of Pediatrics, Stanford School of Medicine, Stanford, California., Beleford D; Institute for Human Genetics and Division of Medical Genetics, Pediatrics, San Francisco, California., Ruzhnikov MRZ; Stanford Center for Undiagnosed Diseases, Stanford University, Stanford, California.; Department of Neurology, Stanford School of Medicine, Stanford, California., Grove ME; Clinical Genomics Program, Stanford Health Care, Stanford, California., Dries AM; Stanford Center for Undiagnosed Diseases, Stanford University, Stanford, California., Kohler JN; Stanford Center for Undiagnosed Diseases, Stanford University, Stanford, California., Waggott DM; Stanford Center for Undiagnosed Diseases, Stanford University, Stanford, California., Yang Y; Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas., Huang Y; Stanford Center for Undiagnosed Diseases, Stanford University, Stanford, California., Mackenzie KM; Department of Neurology, Stanford School of Medicine, Stanford, California., Eng CM; Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas., Fisher PG; Stanford Center for Undiagnosed Diseases, Stanford University, Stanford, California.; Department of Neurology, Stanford School of Medicine, Stanford, California., Ashley EA; Stanford Center for Undiagnosed Diseases, Stanford University, Stanford, California.; Department of Medicine, Stanford University School of Medicine, Stanford, California.; Department of Genetics, Stanford School of Medicine, Stanford, California., Teng JM; Department of Dermatology, Stanford School of Medicine, Stanford, California., Stevenson DA; Department of Pediatrics, Stanford School of Medicine, Stanford, California., Shieh JT; Institute for Human Genetics and Division of Medical Genetics, Pediatrics, San Francisco, California., Wheeler MT; Stanford Center for Undiagnosed Diseases, Stanford University, Stanford, California.; Department of Medicine, Stanford University School of Medicine, Stanford, California., Bernstein JA; Department of Pediatrics, Stanford School of Medicine, Stanford, California.; Stanford Center for Undiagnosed Diseases, Stanford University, Stanford, California.
Publikováno v:
American journal of medical genetics. Part A [Am J Med Genet A] 2019 Jun; Vol. 179 (6), pp. 966-977. Date of Electronic Publication: 2019 Mar 28.
