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Prenatal Screening and Diagnostic Considerations for 22q11.2 Microdeletions.
Blagowidow, Natalie; Nowakowska, Beata; Schindewolf, Erica; Grati, Francesca Romana; Putotto, Carolina; Breckpot, Jeroen; Swillen, Ann; Crowley, Terrence Blaine; Loo, Joanne C Y; Lairson, Lauren A; Óskarsdóttir, Sólveig; Boot, Erik; Garcia-Minaur, Sixto; Cristina Digilio, Maria; Marino, Bruno; Coleman, Beverly; Moldenhauer, Julie S; Bassett, Anne S; McDonald-McGinn, Donna M.
Afiliação
  • Blagowidow N; Harvey Institute for Human Genetics, Greater Baltimore Medical Center, Baltimore, MD 21204, USA.
  • Nowakowska B; Cytogenetic Laboratory, Department of Medical Genetics, Institute of Mother and Child, Kasprzaka 17a, 01-211 Warsaw, Poland.
  • Schindewolf E; Center for Fetal Diagnosis and Treatment and the 22q and You Center, The Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.
  • Grati FR; R&D Department, Menarini Biomarkers Singapore, Via Giuseppe di Vittorio 21/b3, 40013 Castel Maggiore, Italy.
  • Putotto C; Department of Maternal Infantile and Urological Sciences, Sapienza University of Rome (Italy), Viale del Policlinico 155, 00161 Roma, Italy.
  • Breckpot J; Center for Human Genetics, Herestraat 49, 3000 Leuven, Belgium.
  • Swillen A; Center for Human Genetics, Herestraat 49, 3000 Leuven, Belgium.
  • Crowley TB; Division of Human Genetics, The 22q and You Center, and Clinical Genetics Center, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.
  • Loo JCY; The Dalglish Family 22q Clinic, University Health Network, Toronto, ON M5G 2C4, Canada.
  • Lairson LA; Division of Human Genetics, The 22q and You Center, and Clinical Genetics Center, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.
  • Óskarsdóttir S; Department of Paediatrics, Institute of Clinical Sciences, Sahlgrenska Academy, University of Gothenburg, 405 30 Gothenburg, Sweden.
  • Boot E; Department of Paediatrics, Queen Silva Children's Hospital, 416 50 Gothenburg, Sweden.
  • Garcia-Minaur S; The Dalglish Family 22q Clinic, University Health Network, Toronto, ON M5G 2C4, Canada.
  • Cristina Digilio M; Advisium's Heeren Loo, Berkenweg 11, 3818 LA Amersfoort, The Netherlands.
  • Marino B; Department of Psychiatry and Neuropsychology, Maastricht University, 6211 LK Maastricht, The Netherlands.
  • Coleman B; Institute of Medical and Molecular Genetics, Hospital Universitario La Paz, 28046 Madrid, Spain.
  • Moldenhauer JS; Division of Human Genetics, Ospedale Pediatrico Bambino Gesù, IRCCS, 00163 Roma, Italy.
  • Bassett AS; Department of Maternal Infantile and Urological Sciences, Sapienza University of Rome (Italy), Viale del Policlinico 155, 00161 Roma, Italy.
  • McDonald-McGinn DM; Center for Fetal Diagnosis and Treatment and the 22q and You Center, The Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.
Genes (Basel) ; 14(1)2023 01 06.
Article em En | MEDLINE | ID: mdl-36672900
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome de DiGeorge / Doenças Fetais / Cardiopatias Congênitas Tipo de estudo: Diagnostic_studies / Guideline / Prognostic_studies / Screening_studies Limite: Child / Female / Humans / Male / Pregnancy Idioma: En Ano de publicação: 2023 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome de DiGeorge / Doenças Fetais / Cardiopatias Congênitas Tipo de estudo: Diagnostic_studies / Guideline / Prognostic_studies / Screening_studies Limite: Child / Female / Humans / Male / Pregnancy Idioma: En Ano de publicação: 2023 Tipo de documento: Article