Prenatal Screening and Diagnostic Considerations for 22q11.2 Microdeletions.
Saved in:
| Title: | Prenatal Screening and Diagnostic Considerations for 22q11.2 Microdeletions. |
|---|---|
| Authors: | 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.; Department of Paediatrics, Queen Silva Children's Hospital, 416 50 Gothenburg, Sweden., Boot E; The Dalglish Family 22q Clinic, University Health Network, Toronto, ON M5G 2C4, Canada.; Advisium's Heeren Loo, Berkenweg 11, 3818 LA Amersfoort, The Netherlands.; Department of Psychiatry and Neuropsychology, Maastricht University, 6211 LK Maastricht, The Netherlands., Garcia-Minaur S; Institute of Medical and Molecular Genetics, Hospital Universitario La Paz, 28046 Madrid, Spain., Cristina Digilio M; Division of Human Genetics, Ospedale Pediatrico Bambino Gesù, IRCCS, 00163 Roma, Italy., Marino B; Department of Maternal Infantile and Urological Sciences, Sapienza University of Rome (Italy), Viale del Policlinico 155, 00161 Roma, Italy., Coleman B; Center for Fetal Diagnosis and Treatment and the 22q and You Center, The Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.; Department of Radiology, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA., Moldenhauer JS; Center for Fetal Diagnosis and Treatment and the 22q and You Center, The Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.; Department of Obstetrics, Gynecology, and Surgery, Perelman School of Medicine of the University of Pennsylvania, Philadelphia, PA 19104, USA., Bassett AS; The Dalglish Family 22q Clinic, University Health Network, Toronto, ON M5G 2C4, Canada.; Clinical Genetics Research Program and Campbell Family Mental Health Research Institute, Centre for Addiction and Mental Health, and Department of Psychiatry, University of Toronto, Toronto, ON M5S 2S1, Canada.; Division of Cardiology, Department of Medicine, and Centre for Mental Health, and Toronto General Hospital Research Institute, University Health Network, Toronto, ON M5G 2N2, Canada., McDonald-McGinn DM; Division of Human Genetics, The 22q and You Center, and Clinical Genetics Center, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.; Department of Pediatrics, Perelman School of Medicine of the University of Pennsylvania, Philadelphia, PA 19104, USA.; Department of Human Biology and Medical Genetics, Sapienza University, 00185 Roma, Italy. |
| Source: | Genes [Genes (Basel)] 2023 Jan 06; Vol. 14 (1). Date of Electronic Publication: 2023 Jan 06. |
| Publication Type: | Review; Journal Article |
| Journal Info: | Publisher: MDPI Country of Publication: Switzerland NLM ID: 101551097 Publication Model: Electronic Cited Medium: Internet ISSN: 2073-4425 (Electronic) Linking ISSN: 20734425 NLM ISO Abbreviation: Genes (Basel) Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
|
Full text is not displayed to guests.
Login for full access.
|
|
| ISSN: | 2073-4425 |
|---|---|
| DOI: | 10.3390/genes14010160 |
