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Coexisting Conditions Modifying Phenotypes of Patients with 22q11.2 Deletion Syndrome.
Smyk, Marta; Geremek, Maciej; Ziemkiewicz, Kamila; Gambin, Tomasz; Kutkowska-Kazmierczak, Anna; Kowalczyk, Katarzyna; Plaskota, Izabela; Wisniowiecka-Kowalnik, Barbara; Bartnik-Glaska, Magdalena; Niemiec, Magdalena; Grad, Dominika; Piotrowicz, Malgorzata; Gieruszczak-Bialek, Dorota; Pietrzyk, Aleksandra; Crowley, T Blaine; Giunta, Victoria; McGinn, Daniel E; Zackai, Elaine H; Tran, Oanh; Emanuel, Beverly S; McDonald-McGinn, Donna M; Nowakowska, Beata A.
  • Smyk M; Department of Medical Genetics, Institute of Mother and Child, 01-211 Warsaw, Poland.
  • Geremek M; Department of Medical Genetics, Institute of Mother and Child, 01-211 Warsaw, Poland.
  • Ziemkiewicz K; Department of Medical Genetics, Institute of Mother and Child, 01-211 Warsaw, Poland.
  • Gambin T; Department of Medical Genetics, Institute of Mother and Child, 01-211 Warsaw, Poland.
  • Kutkowska-Kazmierczak A; Institute of Computer Science, Warsaw University of Technology, 75, 00-662 Warsaw, Poland.
  • Kowalczyk K; Department of Medical Genetics, Institute of Mother and Child, 01-211 Warsaw, Poland.
  • Plaskota I; Department of Medical Genetics, Institute of Mother and Child, 01-211 Warsaw, Poland.
  • Wisniowiecka-Kowalnik B; Department of Medical Genetics, Institute of Mother and Child, 01-211 Warsaw, Poland.
  • Bartnik-Glaska M; Department of Medical Genetics, Institute of Mother and Child, 01-211 Warsaw, Poland.
  • Niemiec M; Department of Medical Genetics, Institute of Mother and Child, 01-211 Warsaw, Poland.
  • Grad D; Department of Medical Genetics, Institute of Mother and Child, 01-211 Warsaw, Poland.
  • Piotrowicz M; Department of Medical Genetics, Institute of Mother and Child, 01-211 Warsaw, Poland.
  • Gieruszczak-Bialek D; Department of Genetics, Polish Mother's Memorial Hospital Research Institute, 70-445 Lódz, Poland.
  • Pietrzyk A; Department of Medical Genetics, Children's Memorial Health Institute, 04730 Warsaw, Poland.
  • Crowley TB; Department of Genetics and Pathology, Pomeranian Medical University, 70-204 Szczecin, Poland.
  • Giunta V; Division of Human Genetics and 22q and You Center, the Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.
  • McGinn DE; Division of Human Genetics and 22q and You Center, the Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.
  • Zackai EH; Division of Human Genetics and 22q and You Center, the Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.
  • Tran O; Perelman School of Medicine of the University of Pennsylvania, Philadelphia, PA 19104, USA.
  • Emanuel BS; Division of Human Genetics and 22q and You Center, the Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.
  • McDonald-McGinn DM; Perelman School of Medicine of the University of Pennsylvania, Philadelphia, PA 19104, USA.
  • Nowakowska BA; Division of Human Genetics and 22q and You Center, the Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.
Genes (Basel) ; 14(3)2023 03 09.
Article en En | MEDLINE | ID: mdl-36980952
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Síndrome de DiGeorge Límite: Humans Idioma: En Año: 2023 Tipo del documento: Article
Texto completo
Imprimir
XML
PubMed Links
Search on Google

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Síndrome de DiGeorge Límite: Humans Idioma: En Año: 2023 Tipo del documento: Article