Sorath Noorani Siddiqui

Retinoblastoma outcomes in Europe: a prospective analysis of 483 patients from 40 countries

Richard Bowman, Mattan Arazi, Nathalie Cassoux, Allen Foster et autres

gb, il, fr, Maroc, Nigéria, iq, Niger, us, in, pk, id, az, es, ph, sa, cu, Bénin, lb, ye, Égypte, al, se, Mozambique, Libye, it, tr, th, mm, kz, pl, ch, cr, Côte d’Ivoire, Afrique du Sud, de, ua, br, Burkina Faso, Tunisie, Algérie, be, ni, au, py, ie, pt, uy, ar, bg, Tanzanie, mn, nz (code pays fourni par la source)

Ocular Manifestations of Chromosomal Abnormalities

Lorena Haefeli, Sorath Noorani Siddiqui, Alex V. Levin

Increase in blood derived mitochondrial DNA copy number in strabismus patients

Zainab Zehra, Muhammad Amn Zia, Sorath Noorani Siddiqui, Christopher S. von Bartheld et autres

us, pk, qa (code pays fourni par la source)

Exploring WNT2 polymorphisms in comitant strabismus: A genetic association study

Zainab Zehra, Christopher S. von Bartheld, Andrea B. Agarwal, Hans Vasquez-Gross et autres

pk, us, qa (code pays fourni par la source)

Exploring WNT2 Polymorphisms in Comitant Strabismus: A Genetic Association Study

Zainab Zehra, Christopher S. von Bartheld, Andrea B. Agarwal, Hans Vasquez-Gross et autres

pk, us (code pays fourni par la source)

Exploring Wnt2 Polymorphisms in Comitant Strabismus: A Genetic Association Study

Zainab Zehra, Christopher S. von Bartheld, Andrea B. Agarwal, Hans Vasquez-Gross et autres

pk, qa, gb (code pays fourni par la source)

Retinoblastoma in Asia

Swathi Kaliki, Vijitha S. Vempuluru, Ashik Mohamed, Mazin Faisal Al‐Jadiry et autres

in, iq, gb, pk, cn, il, tr, np, th, id, jo (code pays fourni par la source)

Mutation screening of the CYP1B1 gene reveals thirteen novel disease-causing variants in consanguineous Pakistani families causing primary congenital glaucoma

Raeesa Tehreem, Anam Arooj, Sorath Noorani Siddiqui, Shagufta Naz et autres

pk (code pays fourni par la source)

The Global Retinoblastoma Outcome Study: a prospective, cluster-based analysis of 4064 patients from 149 countries

Ido Didi Fabian, Abdallah Elhassan, Shehu U. Abdullahi, Rula Ahmed Abdulqader et autres

Targeted gene sequencing of FYCO1 identified a novel mutation in a Pakistani family for autosomal recessive congenital cataract

Rani Saira Saleem, Sorath Noorani Siddiqui, Saba Irshad, Naeem Mahmood Ashraf et autres

pk, de, nl (code pays fourni par la source)

Association of IGF1 polymorphisms with exotropia in a Pakistani cohort.

Zainab Zehra, Netasha Khan, Minhal Nadeem, Sorath Noorani Siddiqui et autres

us, pk (code pays fourni par la source)

Novel mutations in the PITX2 gene in Pakistani and Mexican families with Axenfeld‐Rieger syndrome

Valeria Lo Faro, Sorath Noorani Siddiqui, Muhammad Imran Khan, Cristina Villanueva‐Mendoza et autres

nl, ps (code pays fourni par la source)