المؤلفون: Hamid Galehdari, Pegah Ghandil, Majid Aminzadeh, Nasrin Malekpour, Gholamreza Shariati

المصدر: Jornal de Pediatria (Versão em Português), Vol 96, Iss 1, Pp 60-65 (2020)
Jornal de Pediatria, Volume: 96, Issue: 1, Pages: 60-65, Published: 02 MAR 2020
Jornal de Pediatria v.96 n.1 2020
Jornal de Pediatria
Sociedade Brasileira de Pediatria (SBP)
instacron:SBPE
Jornal de Pediatria, Vol 96, Iss 1, Pp 60-65 (2020)

مصطلحات موضوعية: Hypoparathyroidism, Population, Prenatal diagnosis, Iran, medicine.disease_cause, Bioinformatics, Osteochondrodysplasias, Asymptomatic, Síndrome HRD, 03 medical and health sciences, 0302 clinical medicine, Seizures, Tubulin, 030225 pediatrics, Intellectual Disability, Genetic variation, medicine, Humans, Abnormalities, Multiple, 030212 general & internal medicine, População iraniana, education, Gene, Gene do cofator E de dobramento da tubulina, Growth Disorders, Mutação, HRD syndrome, Hipoparatireoidismo, Síndrome de Sanjad-Sakati, Fetus, Mutation, education.field_of_study, business.industry, Iranian population, lcsh:RJ1-570, lcsh:Pediatrics, medicine.disease, Sanjad-Sakati syndrome, Pediatrics, Perinatology and Child Health, medicine.symptom, business, Tubulin folding cofactor E gene, Molecular Chaperones

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URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1620022ff1640a5e8a5763b833c241c0
http://www.sciencedirect.com/science/article/pii/S2255553618301976