Multidisciplinary management of a patient with van der Woude syndrome: A case report

nork Tehranchi, Azita, Behnia, Hossein, Nadjmi, Nasser, Yassaee, Vahid Reza, Ravesh, Zeinab, Mina, Morteza
Argitaratua izan da Int J Surg Case Rep (2016)

Advanced molecular approaches pave the road to a clear-cut diagnosis of hereditary retinal dystrophies

nork Ravesh, Zeinab, Dianatpour, Mahdi, Fardaei, Majid, Taghdiri, Maryam, Hashemi-Gorji, Feyzollah, Yassaee, Vahid Reza, Miryounesi, Mohammad
Argitaratua izan da Mol Vis (2018)

Whole exome sequencing and homozygosity mapping reveals genetic defects in consanguineous Iranian families with inherited retinal dystrophies

nork Salmaninejad, Arash, Bedoni, Nicola, Ravesh, Zeinab, Quinodoz, Mathieu, Shoeibi, Nasser, Mojarrad, Majid, Pasdar, Alireza, Rivolta, Carlo
Argitaratua izan da Sci Rep (2020)

Traces of sub-Saharan and Middle Eastern lineages in Indian Muslim populations

nork Eaaswarkhanth, Muthukrishnan, Haque, Ikramul, Ravesh, Zeinab, Romero, Irene Gallego, Meganathan, Poorlin Ramakodi, Dubey, Bhawna, Khan, Faizan Ahmed, Chaubey, Gyaneshwer, Kivisild, Toomas, Tyler-Smith, Chris, Singh, Lalji, Thangaraj, Kumarasamy
Argitaratua 2010

Novel C8orf37 mutations cause retinitis pigmentosa in consanguineous families of Pakistani origin

nork Ravesh, Zeinab, El Asrag, Mohammed E., Weisschuh, Nicole, McKibbin, Martin, Reuter, Peggy, Watson, Christopher M., Baumann, Britta, Poulter, James A., Sajid, Sundus, Panagiotou, Evangelia S., O’Sullivan, James, Abdelhamed, Zakia, Bonin, Michael, Soltanifar, Mehdi, Black, Graeme C.M., Din, Muhammad Amin-ud, Toomes, Carmel, Ansar, Muhammad, Inglehearn, Chris F., Wissinger, Bernd, Ali, Manir
Argitaratua izan da Mol Vis (2015)