Editorial & Opinion
Role of hypocalcemia in identification of 22q11 deletion syndrome among patients with congenital heart defects.
| العنوان: | Role of hypocalcemia in identification of 22q11 deletion syndrome among patients with congenital heart defects. |
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| المؤلفون: | de Mattos VF; Clinical Genetics, Universidade Federal de Ciências da Saúde de Porto Alegre (UFCSPA) and Complexo Hospitalar Santa Casa de Porto Alegre (CHSCPA), RS, Brazil., Sulczinski LP; Graduation in Medicine, Universidade Federal de Ciências da Saúde de Porto Alegre (UFCSPA), RS, Brazil., Milner OG; Graduation in Medicine, Universidade Federal de Ciências da Saúde de Porto Alegre (UFCSPA), RS, Brazil., da Silva FA; Graduation in Medicine, Universidade Federal de Ciências da Saúde de Porto Alegre (UFCSPA), RS, Brazil., de Moraes SA; Graduation in Medicine, Universidade Federal de Ciências da Saúde de Porto Alegre (UFCSPA), RS, Brazil., Trevisan P; Graduate Program in Pathology, Universidade Federal de Ciências da Saúde de Porto Alegre (UFCSPA), RS, Brazil., Fiegenbaum M; Human Genetics, Universidade Federal de Ciências da Saúde de Porto Alegre (UFCSPA), RS, Brazil., Varella-Garcia M; School of Medicine, Division of Medical Oncology, University of Colorado Denver, CO, USA., Zen PR; Clinical Genetics, Universidade Federal de Ciências da Saúde de Porto Alegre (UFCSPA) and Complexo Hospitalar Santa Casa de Porto Alegre (CHSCPA), RS, Brazil; Graduate Program in Pathology, Universidade Federal de Ciências da Saúde de Porto Alegre (UFCSPA), RS, Brazil., Rosa RF; Clinical Genetics, Universidade Federal de Ciências da Saúde de Porto Alegre (UFCSPA) and Complexo Hospitalar Santa Casa de Porto Alegre (CHSCPA), RS, Brazil; Graduate Program in Pathology, Universidade Federal de Ciências da Saúde de Porto Alegre (UFCSPA), RS, Brazil; Clinical Genetics, Hospital Materno Infantil Presidente Vargas (HMIPV), RS, Brazil. Electronic address: rfmr@terra.com.br. |
| المصدر: | International journal of cardiology [Int J Cardiol] 2014 Nov 15; Vol. 177 (1), pp. 6-7. Date of Electronic Publication: 2014 Oct 05. |
| نوع المنشور: | Letter |
| اللغة: | English |
| بيانات الدورية: | Publisher: Elsevier Country of Publication: Netherlands NLM ID: 8200291 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1874-1754 (Electronic) Linking ISSN: 01675273 NLM ISO Abbreviation: Int J Cardiol Subsets: MEDLINE |
| أسماء مطبوعة: | Publication: Amsterdam : Elsevier Original Publication: Amsterdam : Elsevier/North-Holland Biomedical Press, c1981- |
| مواضيع طبية MeSH: | 22q11 Deletion Syndrome/*diagnosis , 22q11 Deletion Syndrome/*genetics , Heart Defects, Congenital/*diagnosis , Heart Defects, Congenital/*genetics , Hypocalcemia/*diagnosis , Hypocalcemia/*genetics, Child, Preschool ; Female ; Humans ; Infant ; Infant, Newborn ; Male |
| فهرسة مساهمة: | Keywords: Calcium; Cardiac malformations; FISH; Screening; Velocardiofacial syndrome |
| تواريخ الأحداث: | Date Created: 20141216 Date Completed: 20150817 Latest Revision: 20141217 |
| رمز التحديث: | 20240628 |
| DOI: | 10.1016/j.ijcard.2014.09.133 |
| PMID: | 25499322 |
| قاعدة البيانات: | MEDLINE |
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Full Text Finder | تدمد: | 1874-1754 |
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| DOI: | 10.1016/j.ijcard.2014.09.133 |