MEIS2 (15q14) gene deletions in siblings with mild developmental phenotypes and bifid uvula: documentation of mosaicism in an unaffected parent

por Zhang, Bin, Liu, Michel, Fong, Chin-To, Iqbal, M. Anwar
Publicado 2021

Cytogenetics and etiology of ambiguous genitalia in 120 pediatric patients

por Al-Mutair, Angham, Iqbal, M. Anwar, Sakati, Nadia, Ashwal, Abdullah
Publicado 2004

Novel 1.3 Mb germline duplication in chromosome 8q21.11 by microarray comparative genomic hybridization plus single nucleotide polymorphism analysis in an adult patient with pancyt...

por Reyes Barron, Cynthia, Evans, Andrew G., Miyamoto, Hiroshi, Zhang, Bin, Iqbal, M. Anwar
Publicado 2018

Allelic and dosage effects of NHS in X-linked cataract and Nance–Horan syndrome: a family study and literature review

por Miller, Caroline, Gertsen, Benjamin G., Schroeder, Audrey L., Fong, Chin-To, Iqbal, M. Anwar, Zhang, Bin
Publicado 2021

Renal Failure Associated with APECED and Terminal 4q Deletion: Evidence of Autoimmune Nephropathy

por Al-Owain, Mohammed, Kaya, Namik, Al-Zaidan, Hamad, Bin Hussain, Ibrahim, Al-Manea, Hadeel, Al-Hindi, Hindi, Kennedy, Shelley, Iqbal, M. Anwar, Al-Mojalli, Hamad, Al-Bakheet, Albandary, Puel, Anne, Casanova, Jean-Laurent, Al-Muhsen, Saleh
Publicado 2010