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M Anwar Iqbal

Showing results (1-10 of 25) with videos related to

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Current Medicinal Chemistry|June 12, 2012
Significance of genome-wide analysis of copy number alterations and UPD in myelodysplastic syndromes using combined CGH - SNP arraysAusaf Ahmad, M Anwar Iqbal
American Journal of Medical Genetics. Part A|July 17, 2007
Interstitial del(20)(q11.2q12) - clinical and molecular cytogenetic characterizationM Anwar Iqbal, Mohammad Al-Owain
Prenatal Diagnosis|October 22, 2005
Complex de novo cryptic subtelomeric rearrangements in a fetus with multiple ultrasonographic abnormalities and a normal karyotype at amniocentesisM Anwar Iqbal, Sahar Ramadan, Faten Al Ali, et al.
Annals of Saudi Medicine|December 3, 2004
Cytogenetics and etiology of ambiguous genitalia in 120 pediatric patientsAngham Al-Mutair, M Anwar Iqbal, Nadia Sakati, et al.
Molecular Cytogenetics|December 21, 2021
MEIS2 (15q14) gene deletions in siblings with mild developmental phenotypes and bifid uvula: documentation of mosaicism in an unaffected parentBin Zhang, Michel Liu, Chin-To Fong, et al.
International Journal of Radiation Biology|May 9, 2012
Radiation effects on human leptomeningeal cell response to cerebrospinal fluid and PDGF-BBMahlon D Johnson, Mary O'Connell, M Anwar Iqbal, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|July 9, 2016
Combined comparative genomic hybridization and single-nucleotide polymorphism array detects cryptic chromosomal lesions in both myelodysplastic syndromes and cytopenias of undetermined significanceAndrew G Evans, Ausaf Ahmad, W Richard Burack, et al.
Molecular Cytogenetics|December 19, 2025
Optical genome mapping identifies novel ENOX2::RUNX1 t(X;21)(q26.1;q22.12) rearrangement in acute myeloid leukemia-myelodysplasia related: first case reportGiby V George, Sarmad Ali, Chauncey R Syposs, et al.
Clinical Case Reports|October 24, 2018
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 complicationsCynthia Reyes Barron, Andrew G Evans, Hiroshi Miyamoto, et al.
Genes|January 25, 2025
Utilization of RT-PCR and Optical Genome Mapping in Acute Promyelocytic Leukemia with Cryptic <i>PML::RARA</i> Rearrangement: A Case Discussion and Systemic Literature ReviewGiby V George, Murad Elsadawi, Andrew G Evans, et al.
Pageof 3

Showing results (1-10 of 25) with videos related to

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Pageof 3
Current Medicinal Chemistry|June 12, 2012
Significance of genome-wide analysis of copy number alterations and UPD in myelodysplastic syndromes using combined CGH - SNP arraysAusaf Ahmad, M Anwar Iqbal
American Journal of Medical Genetics. Part A|July 17, 2007
Interstitial del(20)(q11.2q12) - clinical and molecular cytogenetic characterizationM Anwar Iqbal, Mohammad Al-Owain
Prenatal Diagnosis|October 22, 2005
Complex de novo cryptic subtelomeric rearrangements in a fetus with multiple ultrasonographic abnormalities and a normal karyotype at amniocentesisM Anwar Iqbal, Sahar Ramadan, Faten Al Ali, et al.
Annals of Saudi Medicine|December 3, 2004
Cytogenetics and etiology of ambiguous genitalia in 120 pediatric patientsAngham Al-Mutair, M Anwar Iqbal, Nadia Sakati, et al.
Molecular Cytogenetics|December 21, 2021
MEIS2 (15q14) gene deletions in siblings with mild developmental phenotypes and bifid uvula: documentation of mosaicism in an unaffected parentBin Zhang, Michel Liu, Chin-To Fong, et al.
International Journal of Radiation Biology|May 9, 2012
Radiation effects on human leptomeningeal cell response to cerebrospinal fluid and PDGF-BBMahlon D Johnson, Mary O'Connell, M Anwar Iqbal, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|July 9, 2016
Combined comparative genomic hybridization and single-nucleotide polymorphism array detects cryptic chromosomal lesions in both myelodysplastic syndromes and cytopenias of undetermined significanceAndrew G Evans, Ausaf Ahmad, W Richard Burack, et al.
Molecular Cytogenetics|December 19, 2025
Optical genome mapping identifies novel ENOX2::RUNX1 t(X;21)(q26.1;q22.12) rearrangement in acute myeloid leukemia-myelodysplasia related: first case reportGiby V George, Sarmad Ali, Chauncey R Syposs, et al.
Clinical Case Reports|October 24, 2018
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 complicationsCynthia Reyes Barron, Andrew G Evans, Hiroshi Miyamoto, et al.
Genes|January 25, 2025
Utilization of RT-PCR and Optical Genome Mapping in Acute Promyelocytic Leukemia with Cryptic <i>PML::RARA</i> Rearrangement: A Case Discussion and Systemic Literature ReviewGiby V George, Murad Elsadawi, Andrew G Evans, et al.
Pageof 3