Prenatal cardiac findings and 22q11.2 deletion syndrome: Fetal detection and evaluation.
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| Title: | Prenatal cardiac findings and 22q11.2 deletion syndrome: Fetal detection and evaluation. |
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| Authors: | Goldmuntz E; Division of Cardiology, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.; Department of Pediatrics, Perelman School of Medicine of the University of Pennsylvania, Philadelphia, Pennsylvania, USA., Bassett AS; The Dalglish Family 22q Clinic, Toronto General Hospital, University Health Network, Toronto, Ontario, Canada.; Clinical Genetics Research Program, Centre for Addiction and Mental Health, Toronto, Ontario, Canada.; Campbell Family Mental Health Research Institute, Centre for Addiction and Mental Health, Toronto, Ontario, Canada.; Department of Psychiatry, University of Toronto, Toronto, Ontario, Canada., Boot E; The Dalglish Family 22q Clinic, Toronto General Hospital, University Health Network, Toronto, Ontario, Canada.; Advisium, 's Heeren Loo Zorggroep, Amersfoort, The Netherlands.; Department of Psychiatry and Neuropsychology, Maastricht University, Maastricht, The Netherlands., Marino B; Department of Maternal Infantile and Urological Sciences, Sapienza University of Rome (Italy), Roma, Italy., Moldenhauer JS; Division of Human Genetics, 22q and You Center, Clinical Genetics Center, Section of Genetic Counseling, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.; Departments of Obstetrics and Gynecology and Surgery, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania, USA., Óskarsdóttir S; Department of Pediatrics, Institute of Clinical Sciences, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.; Department of Rheumatology and Immunology, Queen Silvia Children's Hospital, Gothenburg, Sweden., Putotto C; Department of Maternal Infantile and Urological Sciences, Sapienza University of Rome (Italy), Roma, Italy., Rychik J; Division of Cardiology, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.; Department of Pediatrics, Perelman School of Medicine of the University of Pennsylvania, Philadelphia, Pennsylvania, USA., Schindewolf E; Division of Human Genetics, 22q and You Center, Clinical Genetics Center, Section of Genetic Counseling, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA., McDonald-McGinn DM; Department of Pediatrics, Perelman School of Medicine of the University of Pennsylvania, Philadelphia, Pennsylvania, USA.; Division of Human Genetics, 22q and You Center, Clinical Genetics Center, Section of Genetic Counseling, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.; Department of Human Biology and Medical Genetics, Sapienza University, Rome, Italy., Blagowidow N; The Harvey Institute for Human Genetics, Greater Baltimore Medical Center, Baltimore, Maryland, USA. |
| Source: | Prenatal diagnosis [Prenat Diagn] 2024 Jun; Vol. 44 (6-7), pp. 804-814. Date of Electronic Publication: 2024 Apr 09. |
| Publication Type: | Journal Article; Review; Research Support, N.I.H., Extramural |
| Journal Info: | Publisher: Wiley Country of Publication: England NLM ID: 8106540 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1097-0223 (Electronic) Linking ISSN: 01973851 NLM ISO Abbreviation: Prenat Diagn Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
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| ISSN: | 1097-0223 |
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| DOI: | 10.1002/pd.6566 |
