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

المصدر: Jornal de Pediatria (Versão em Português), Vol 96, Iss 1, Pp 60-65 (2020)

مصطلحات موضوعية: Pediatrics, RJ1-570

وصف الملف: electronic resource

Relation: http://www.sciencedirect.com/science/article/pii/S2255553618301976; https://doaj.org/toc/2255-5536

URL الوصول: https://doaj.org/article/2f3fa6b3819841979a2fe60ad262b4bf

المؤلفون: Nasrin Malekpour, Rahim Vakili, Tayebeh Hamzehloie

المصدر: Iranian Journal of Basic Medical Sciences, Vol 21, Iss 9, Pp 950-956 (2018)

مصطلحات موضوعية: ARSB gene, Arylsulfatase B, Consanguineous marriage, DNA sequencing, Maroteaux-Lamy syndrome, Mucopolysaccharidosis VI (MPS VI), Medicine

وصف الملف: electronic resource

Relation: http://ijbms.mums.ac.ir/article_11251_92da38c0dc480568787e925f69546db3.pdf; https://doaj.org/toc/2008-3866; https://doaj.org/toc/2008-3874

URL الوصول: https://doaj.org/article/ae8d97442aff4d08a29c2f63ad7b941b

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

وصف الملف: text/html

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

المؤلفون: Nasrin Malekpour, Pegah Ghandil, Majid Aminzadeh

المصدر: Gene. 706

مصطلحات موضوعية: 0301 basic medicine, Arylsulfatase B, Adult, Male, N-Acetylgalactosamine-4-Sulfatase, Mucopolysaccharidosis, Population, Nonsense mutation, DNA Mutational Analysis, Gene mutation, Biology, Iran, 03 medical and health sciences, Consanguinity, 0302 clinical medicine, Genetics, medicine, Missense mutation, Humans, education, education.field_of_study, Mucopolysaccharidosis VI, General Medicine, DNA, Exons, Sequence Analysis, DNA, medicine.disease, Maroteaux–Lamy syndrome, 030104 developmental biology, Phenotype, 030220 oncology & carcinogenesis, Mutation, Female

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8d4d2cda84beaa316b461a9aa7d3c754
https://pubmed.ncbi.nlm.nih.gov/31009684

المؤلفون: Shima Ardekhani, Samane Heidarzade, Nasrin Malekpour, Seyed Mohammad Amin Kormi

المصدر: Journal of Genes and Cells. 3:1

مصطلحات موضوعية: Cancer stem cell, Cancer research, medicine, Cancer, Biology, Stem cell, medicine.disease

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::227d13949f8cc6d6ffbbdf1ca80683e7
https://doi.org/10.15562/gnc.48