-
1دورية أكاديمية
لا يتم عرض هذه النتيجة على الضيوف.
تسجيل الدخول للوصول الكامل. -
2دورية أكاديمية
المؤلفون: Mestre VF, Spoladori IC, Osiak LB, Paiva WJM, Ferreira de Lima RL, Silveira BC, Salles MJS
المصدر: General dentistry [Gen Dent] 2022 Jul-Aug; Vol. 70 (4), pp. 59-66.
نوع المنشور: Journal Article
بيانات الدورية: Publisher: Academy of General Dentistry Country of Publication: United States NLM ID: 7610466 Publication Model: Print Cited Medium: Internet ISSN: 0363-6771 (Print) Linking ISSN: 03636771 NLM ISO Abbreviation: Gen Dent
مواضيع طبية MeSH: Cleidocranial Dysplasia*/diagnostic imaging , Cleidocranial Dysplasia*/genetics, Core Binding Factor Alpha 1 Subunit/genetics ; Humans
-
3تقرير
المؤلفون: Osiak L; Laboratory of Developmental Toxicology, Department of General Biology, State University of Londrina., Saraiva JG; Laboratory of Developmental Toxicology, Department of General Biology, State University of Londrina., Mestre VF; Laboratory of Developmental Toxicology, Department of General Biology, State University of Londrina., Ferrari LSL; Department of Pediatrics and Pediatric Surgery, State University of Londrina., Paiva WJM; Genetic Counseling Service, Department of General Biology, State University of Londrina, Londrina, Paraná., de Lima RLLF; Human Genetics and Mutagenesis Laboratory, Department of Genetics, Institute of Biology, Federal University of Bahia, Salvador, Brazil., Salles MJS; Laboratory of Developmental Toxicology, Department of General Biology, State University of Londrina.
المصدر: Clinical dysmorphology [Clin Dysmorphol] 2020 Jul; Vol. 29 (3), pp. 165-166.
نوع المنشور: Case Reports; Letter
بيانات الدورية: Publisher: Lippincott Williams & Wilkins Country of Publication: England NLM ID: 9207893 Publication Model: Print Cited Medium: Internet ISSN: 1473-5717 (Electronic) Linking ISSN: 09628827 NLM ISO Abbreviation: Clin Dysmorphol Subsets: MEDLINE
مواضيع طبية MeSH: Monosomy/*genetics, Child, Preschool ; Chromosome Deletion ; Chromosomes, Human, Pair 21/genetics ; Female ; Humans ; Infant
SCR Disease Name: Chromosome 21 monosomy
Full Text Finder