Prevalence of human papilloma virus (HPV) genotypes between outpatients males and females referred to seven laboratories in Tehran, Iran von Rezaee Azhar, Iman, Yaghoobi, Mahmood, Mossalaeie, Mir Majid, Kollaee Darabi, Abolghasem, Nejadeh, Amir Houshang, Jamshidi, Mahbobeh, Ahani, Ali, Karkhane Mahmoodi, Masoud, Ghalichi, Leila, Shabanzadeh, Ayda, Ataei-Pirkooh, Angila, Marjani, Arezoo, Khamseh, Azam, Shafiei, Motahareh, Hosseini, Parastoo, Soltani, Saber, Zandi, Milad, Ghafari, Parsa, Aboofazeli, Amir, Ghaziasadi, Azam, Jazayeri, Seyed Mohammad

Volltext

The influence of combined genotypes of the HLADRB11501 and CD24 single nucleotide polymorphism on disease severity of Iranian multiple sclerosis patients von Ghlichnia, Hossein Ali, Kollaee, Abolghasem, Gaffarpoor, Majid, Movafagh, Abolfazl, Ghlichnia, Babak, Zamani, Mahdi

Volltext

Exome sequencing found a novel homozygous deletion in ADCK3 gene involved in autosomal recessive spinocerebellar ataxia von Hajjari, Mohammadreza, Tahmasebi-Birgani, Maryam, Mohammadi-asl, Javad, Nasiri, Habib, Kollaee, Abolghasem, Mahmoodi, Mandana, Ansari, Hossein

Volltext

Exome sequencing revealed a p.G299R mutation in the COMP gene in an Iranian family suffering from pseudoachondroplasia von Ansari, Hossein, Mohammadi‐Asl, Javad, Hajjari, Mohammadreza, Tahmasebi‐Birgani, Maryam, Kollaee, Abolghasem, Jassemi‐zergani, Farzad, Vakili‐Hajiagha, Amin

Volltext