M. Iqbal

发表

Significance of genome-wide analysis of copy number alterations and UPD in myelodysplastic syndromes using combined CGH - SNP arrays.

Ausaf Ahmad, M. Iqbal, 2012, Current medicinal chemistry.

Assessing copy number aberrations and copy neutral loss of heterozygosity across the genome as best practice: An evidence based review of clinical utility from the cancer genomics consortium (CGC) working group for myelodysplastic syndrome, myelodysplastic/myeloproliferative and myeloproliferative n

M. Slovak, F. Quintero-Rivera, G. Raca, 2018, Cancer genetics.

Isodicentric Philadelphia chromosomes in imatinib mesylate (Gleevec)-resistant patients.

J. Liesveld, J. O'Malley, M. Iqbal, 2007, Cancer genetics and cytogenetics.

Combined comparative genomic hybridization and single-nucleotide polymorphism array detects cryptic chromosomal lesions in both myelodysplastic syndromes and cytopenias of undetermined significance

W. R. Burack, Ausaf Ahmad, A. Evans, 2016, Modern Pathology.

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

C. Fong, M. Iqbal, Bin Zhang, 2021, Molecular Cytogenetics.

Pathogenetics of alveolar capillary dysplasia with misalignment of pulmonary veins

Kristin M. Scheible, U. Surti, P. Stankiewicz, 2016, Human Genetics.

ICF Syndrome in Saudi Arabia: Immunological, Cytogenetic and Molecular Analysis

A. Al-ghonaium, N. Kaya, D. Çolak, 2011, Journal of Clinical Immunology.

Disruption of normal patterns of FOXF1 expression in a lethal disorder of lung development

Kristin M. Scheible, P. Stankiewicz, P. Szafranski, 2019, Journal of Medical Genetics.

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

C. Fong, M. Iqbal, A. Schroeder, 2021, Molecular cytogenetics.

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

C. Fong, M. Iqbal, Bin Zhang, 2021, Molecular Cytogenetics.

A 0.7 Mb de novo duplication at 7q21.3 including the genes DLX5 and DLX6 in a patient with split‐hand/split‐foot malformation

M. Velinov, Ausaf Ahmad, M. Iqbal, 2012, American journal of medical genetics. Part A.

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 pancytopenia and urinary bladder complications

H. Miyamoto, Bin Zhang, A. Evans, 2018, Clinical case reports.