A case report of 22q11 deletion syndrome confirmed by array-CGH method

Por Sedghi, Maryam, Nouri, Narges, Abdali, Hossein, Memarzadeh, Mehrdad, Nouri, Nayereh
Publicado em 2012

A Novel Mutation in the Aprataxin (APTX) Gene in an Iranian Individual Suffering Early-Onset Ataxia with Oculomotor Apraxia Type 1(AOA1) Disease

Por Nouri, Nayereh, Nouri, Narges, Aryani, Omid, Kamalidehghan, Behnam, Sedghi, Maryam, Houshmand, Massoud
Publicado em 2012

Identification of Proximal and Distal 22q11.2 Microduplications among Patients with Cleft Lip and/or Palate: A Novel Inherited Atypical 0.6 Mb Duplication

Por Sedghi, Maryam, Abdali, Hossein, Memarzadeh, Mehrdad, Salehi, Mansoor, Nouri, Narges, Hosseinzadeh, Majid, Nouri, Nayereh
Publicado no Genet Res Int (2015)

Prevalence of 22q11.2 microdeletion syndrome in Iranian patients with cleft palate

Por Nouri, Narges, Memarzadeh, Mehrdad, Salehi, Mansoor, Nouri, Nayereh, Meamar, Rokhsareh, Behnam, Mahdiyeh, Derakhshandeh, Fatemeh, Kashkoolinejad, Tahereh, Abdali, Hossein
Publicado no Adv Biomed Res (2016)

Two novel homozygous RAB3GAP1 mutations cause Warburg micro syndrome

Por Imagawa, Eri, Fukai, Ryoko, Behnam, Mahdiyeh, Goyal, Manisha, Nouri, Narges, Nakashima, Mitsuko, Tsurusaki, Yoshinori, Saitsu, Hirotomo, Salehi, Mansour, Kapoor, Seema, Tanaka, Fumiaki, Miyake, Noriko, Matsumoto, Naomichi
Publicado no Hum Genome Var (2015)