Does PTEN gene mutation play any role in Li-Fraumeni syndrome

por Akouchekian, Mansoureh, Hemati, Simin, Jafari, Davood, Jalilian, Nazanin, Dehghan Manshadi, Masoumeh
Publicado 2016

Cytogenetic Analysis of 570 Couples with Recurrent Pregnancy Loss: Reporting 11 Years of Experience

por Alibakhshi, Reza, Nejati, Parham, Hamani, Sara, Mir-Ahadi, Narges, Jalilian, Nazanin
Publicado 2020

p53 p.Pro72Arg (rs1042522) and Mouse Double Minute 2 (MDM2) Single-Nucleotide Polymorphism (SNP) 309 Variants and Their Interaction in Chronic Lymphocytic Leukemia(CLL): A Survey i...

por Jalilian, Nazanin, Maleki, Yosra, Shakiba, Ebrahim, Aznab, Mozafar, Rahimi, Ziba, Salimi, Mehdi, Rhimi, Zohreh
Publicado 2021

A Comprehensive Genetic and Clinical Evaluation of Waardenburg Syndrome Type II in a Set of Iranian Patients

por Jalilian, Nazanin, Tabatabaiefar, Mohammad Amin, Yazdanpanah, Mahboubeh, Darabi, Elham, Bahrami, Tayyeb, Zekri, Ali, Noori-Daloii, Mohammad Reza
Publicado 2018

Molecular and clinical characterization of autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome (APECED) in Iranian non-Jewish patients: report of two novel AIRE...

por Setoodeh, Aria, Panjeh-Shahi, Samareh, Bahmani, Fariba, Vand-Rajabpour, Fatemeh, Jalilian, Nazanin, Sayarifard, Fatemeh, Abbasi, Farzaneh, Sayarifard, Azadeh, Rostami, Parastoo, Parvaneh, Nima, Akhavan-Niaki, Haleh, Ahmadifard, Mohamadreza, Tabrizi, Mina
Publicado 2022