Screening of the LAMB2, WT1, NPHS1, and NPHS2 Genes in Pediatric Nephrotic Syndrome

por Abid, Aiysha, Shahid, Saba, Shakoor, Madiha, Lanewala, Ali A., Hashmi, Seema, Khaliq, Shagufta
Publicado 2018

Genetic Alterations, DNA Methylation, Alloantibodies and Phenotypic Heterogeneity in Type III von Willebrand Disease

por Naveed, Muhammad Asif, Abid, Aiysha, Ali, Nadir, Hassan, Yaqoob, Amar, Ali, Javed, Aymen, Qamar, Khansa, Mustafa, Ghulam, Raza, Ali, Saleem, Umera, Hussain, Shabbir, Shakoor, Madiha, Khaliq, Shagufta, Mohsin, Shahida
Publicado 2022