Prenatal diagnosis in a mentally retarded woman with mosaic ring chromosome 18

od Bagherizadeh, Eiman, Behjati, Farkhondeh, Saberi, Seyed Hoseinali, Shafeghati, Yousef
Izdano 2011

Fanconi-Bickel syndrome versus osteogenesis imperfeeta: An Iranian case with a novel mutation in glucose transporter 2 gene, and review of literature

od Hadipour, Fatemeh, Sarkheil, Peymaneh, Noruzinia, Mehrdad, Hadipour, Zahra, Baghdadi, Taghi, Shafeghati, Yousef
Izdano 2013

Evaluation of Methylation Status in the 5'UTR Promoter Region of the DBC2 Gene as a Biomarker in Sporadic Breast Cancer

od Hajikhan Mirzaei, Mehri, Noruzinia, Mehrdad, Karbassian, Hamid, Shafeghati, Yousef, Keyhanee, Mousa, Bidmeshki-Pour, Ali
Izdano 2012

Phenotypic Overlap of Roberts and Baller-Gerold Syndromes in Two Patients With Craniosynostosis, Limb Reductions, and ESCO2 Mutations

od Colombo, Elisa Adele, Mutlu-Albayrak, Hatice, Shafeghati, Yousef, Balasar, Mine, Piard, Juliette, Gentilini, Davide, Di Blasio, Anna Maria, Gervasini, Cristina, Van Maldergem, Lionel, Larizza, Lidia
Izdano u Front Pediatr (2019)

Whole-Exome Sequencing Identifies Three Candidate Homozygous Variants in a Consanguineous Iranian Family with Autism Spectrum Disorder and Skeletal Problems

od Farajzadeh Valilou, Saeed, Alavi, Afagh, Pashaei, Mahdiyeh, Ghasemi Firouzabadi, Saghar, Shafeghati, Yousef, Nozari, Ahoura, Hadipour, Fatemeh, Hadipour, Zahra, Maghsoodlou Estrabadi, Bijan, Gholamreza Noorazar, Seyed, Banihashemi, Susan, Karimian, Javad, Fattahi, Mahshid, Behjati, Farkhondeh
Izdano u Mol Syndromol (2020)

Investigation of Chromosomal Abnormalities and Microdeletion/ Microduplication(s) in Fifty Iranian Patients with Multiple Congenital Anomalies

od Mohammadzadeh, Akbar, Akbaroghli, Susan, Aghaei-Moghadam, Ehsan, Mahdieh, Nejat, Badv, Reza Shervin, Jamali, Payman, Kariminejad, Roxana, Chavoshzadeh, Zahra, Ghasemi Firouzabadi, Saghar, Mansour Ghanaie, Roxana, Nozari, Ahoura, Banihashemi, Sussan, Hadipour, Fatemeh, Hadipour, Zahra, Kariminejad, Ariana, Najmabadi, Hossein, Shafeghati, Yousef, Behjati, Farkhondeh
Izdano u Cell J (2019)

Identification of Chromosome Abnormalities in Subtelomeric Regions Using Multiplex Ligation Dependent Probe Amplification (MLPA) Technique in 100 Iranian Patients With Idiopathic M...

od Behjati, Farkhondeh, Ghasemi Firouzabadi, Saghar, Sajedi, Firoozeh, Kahrizi, Kimia, Najafi, Mostafa, Ebrahimizade Ghasemlou, Behruz, Shafeghati, Yousef, Behnia, Fatemeh, Mohammadi Arya, Ali Reza, Karimi, Hossein, Hadipour, Fatemeh, Hadipour, Zahra, Jamali, Peyman, Kariminejad, Roxana, Darvish, Hossein, Bahman, Ideh, Bagherizadeh, Eiman, Najmabadi, Hossein, Vameghi, Roshanak
Izdano 2013

Identification of CANT1 Mutations in Desbuquois Dysplasia

od Huber, Céline, Oulès, Bénédicte, Bertoli, Marta, Chami, Mounia, Fradin, Mélanie, Alanay, Yasemin, Al-Gazali, Lihadh I., Ausems, Margreet G.E.M., Bitoun, Pierre, Cavalcanti, Denise P., Krebs, Alexander, Le Merrer, Martine, Mortier, Geert, Shafeghati, Yousef, Superti-Furga, Andrea, Robertson, Stephen P., Le Goff, Carine, Muda, Andrea Onetti, Paterlini-Bréchot, Patrizia, Munnich, Arnold, Cormier-Daire, Valérie
Izdano 2009

A molecular and clinical study of Larsen syndrome caused by mutations in FLNB

od Bicknell, Louise S, Farrington‐Rock, Claire, Shafeghati, Yousef, Rump, Patrick, Alanay, Yasemin, Alembik, Yves, Al‐Madani, Navid, Firth, Helen, Karimi‐Nejad, Mohammad Hassan, Kim, Chong Ae, Leask, Kathryn, Maisenbacher, Melissa, Moran, Ellen, Pappas, John G, Prontera, Paolo, de Ravel, Thomy, Fryns, Jean‐Pierre, Sweeney, Elizabeth, Fryer, Alan, Unger, Sheila, Wilson, L C, Lachman, Ralph S, Rimoin, David L, Cohn, Daniel H, Krakow, Deborah, Robertson, Stephen P
Izdano 2007