Excessive homozygosity identified by chromosomal microarray at a known GCDH mutation locus correlates with brain MRI abnormalities in an infant with glutaric aciduria

por Peer‐Zada, Abdul Ali, Al‐Asmari, Ali M.
Publicado 2017

Atypical presentation of adenosine deaminase 2 deficiency with bi‐allelic ADA2 mutation

por Al‐shaikh, Reem, Alnowaiser, Dimah, Peer‐Zada, Abdul Ali, Almutairi, Awatif, Alghamdi, Hamza
Publicado 2022

The evaluation of DiGeorge syndrome gene deletion using molecular cytogenetic techniques

por Bahamat, Abeer A, Lary, Sahira A, Peer Zada, Abdul Ali, AL-Qahtani, Mohammed H
Publicado 2014

Development of simple and effective PCR based assay to detect PCCA mutation (c.425G > A) among Saudi carriers and functional study of the homozygous PCCA mutations

por Al-Asmari, Ali, Peer-Zada, Abdul Ali, AlDehaimi, Abdulwahed, Polychronakos, Constantin, Chentoufi, Aziz A.
Publicado 2022

Fatal intracranial haemorrhage in acute promyelocytic leukemia patients with short isoform of PML-RARα: Review of molecular and radiological data

por Abudawood, Manal, Alorini, Hanan, Samman, Manar A., Bashir, Salman M., AlSwayed, Azizah, Binhassan, Sarah, Peer-Zada, Abdul Ali
Publicado 2023

Favorable outcome of PML‐RARα short isoform and FLT3‐ITD mutation in a patient with several adverse prognostic markers: A case report

por Bafail, Mohammed A., AlTahan, Rahaf, Samman, Manar A., Tashkandi, Suha A., Motabi, Ibraheem H., Peer‐Zada, Abdul Ali
Publicado 2023