22q11.2 Deletion Syndrome in Patients Admitted to a Cardiac Pediatric Intensive Care Unit in Brazil
- Author
- ROSA, Rafael F. M1 2 3 ; PILLA, Carlo B4 ; PASKULIN, Giorgio A1 2 3 ; PEREIRA, Vera L. B2 ; FLORES, José A. M5 ; GOLENDZINER, Eliete5 ; KOSHIYAMA, Dayane B2 ; HERTZ, Michele T2 ; RICACHINEVSKY, Claudia P4 ; ROMAN, Tatiana2 3 ; VARELLA-GARCIA, Marileila6
[1] Clinical Genetics, Universidade Federal de Ciências da Saúde de Porto Alegre (UFCSPA) and Complexo Hospitalar Santa Casa de Porto Alegre (CHSCPA), Porto Alegre, RS, Brazil
[2] Department of Morphological Sciences, UFCSPA, Porto Alegre, RS, Brazil
[3] Graduate Program in Pathology, UFCSPA, Porto Alegre, RS, Brazil
[4] Departments of Pediatric Cardiology, Intensive Care, and Cardiac Surgery, Hospital da Criança Santo Antônio (HCSA), CHSCPA, Porto Alegre, RS, Brazil
[5] Department of Pediatric Radiology, HCSA, CHSCPA, Porto Alegre, RS, Brazil
[6] Department of Medicine, Division of Medical Oncology, University of Colorado Denver, Aurora, Colorado, United States - Source
American journal of medical genetics. Part A. 2008, Vol 146, Num 13, pp 1655-1661, 7 p ; ref : 1 p
- Publisher
- Wiley-Liss, Hoboken, NJ
- Publication country
- United States
- Document type
- Article
- Language
- English
- Author keyword
- 22q11.2 deletion syndrome 22q11.2 microdeletion DiGeorge syndrome FISH chromosome 22 congenital heart defects conotruncal heart defects
- Keyword (fr)
- Cardiopathie congénitale Chromosome G22 Coeur Enfant Homme Hybridation in situ fluorescence Immunodéficit héréditaire de Di George Syndrome vélocardiofacial Unité soin intensif Microdélétion Brésil Immunopathologie Pathologie de l'appareil circulatoire Amérique du Sud Amérique
- Keyword (en)
- Congenital cardiopathy Chromosome G22 Heart Child Human Fluorescence in situ hybridization Di George's syndrome Velocardiofacial syndrome Intensive care unit Microdeletion Brazil Immunopathology Cardiovascular disease South America America
- Keyword (es)
- Cardiopathía congénita Cromosoma G22 Corazón Niño Hombre Hibridación in situ fluorescencia Inmunodeficiencia hereditaria Di George Velocardiofacial síndrome Unidad terapia intensiva Microdeletion Brasil Inmunopatología Aparato circulatorio patología America del sur America
- Classification
- Discipline
- Medical genetics
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 20452320
Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS
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DOI
10.1002/ajmg.a.32378 
https://dx.doi.org/10.1002/ajmg.a.32378
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