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

ανά Tehranchi, Azita, Behnia, Hossein, Nadjmi, Nasser, Yassaee, Vahid Reza, Ravesh, Zeinab, Mina, Morteza
Τόπος έκδοσης Int J Surg Case Rep (2016)

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

ανά Ravesh, Zeinab, Dianatpour, Mahdi, Fardaei, Majid, Taghdiri, Maryam, Hashemi-Gorji, Feyzollah, Yassaee, Vahid Reza, Miryounesi, Mohammad
Τόπος έκδοσης Mol Vis (2018)

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

ανά Salmaninejad, Arash, Bedoni, Nicola, Ravesh, Zeinab, Quinodoz, Mathieu, Shoeibi, Nasser, Mojarrad, Majid, Pasdar, Alireza, Rivolta, Carlo
Τόπος έκδοσης Sci Rep (2020)

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

ανά 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
Έκδοση 2010

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

ανά 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
Τόπος έκδοσης Mol Vis (2015)