M Anwar Iqbal

Summary

Affiliation: King Faisal Specialist Hospital and Research Centre
Country: Saudi Arabia

Publications

  1. ncbi request reprint Complex de novo cryptic subtelomeric rearrangements in a fetus with multiple ultrasonographic abnormalities and a normal karyotype at amniocentesis
    M Anwar Iqbal
    Section of Cytogenetics Molecular Genetics, Department of Pathology and Laboratory Medicine, King Faisal Specialist Hospital and Research Center, Riyadh, Kingdom of Saudi Arabia
    Prenat Diagn 25:1142-9. 2005
  2. ncbi request reprint del(6)(p23) in two cases of de novo AML--a new recurrent primary chromosome abnormality
    M Anwar Iqbal
    Section of Cytogenetics Molecular Genetics, Department of Pathology and Laboratory Medicine, King Faisal Cancer Center, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia
    Eur J Haematol 77:245-50. 2006
  3. ncbi request reprint Interstitial del(20)(q11.2q12) - clinical and molecular cytogenetic characterization
    M Anwar Iqbal
    Cytogenetics and Molecular Cytogenetics, Department of Pathology and Laboratory Medicine, Saudi Arabia
    Am J Med Genet A 143:1880-4. 2007
  4. ncbi request reprint Cytogenetics and etiology of ambiguous genitalia in 120 pediatric patients
    Angham Al-Mutair
    Department of Pediatrics, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia
    Ann Saudi Med 24:368-72. 2004
  5. ncbi request reprint Isodicentric Philadelphia chromosomes in imatinib mesylate (Gleevec)-resistant patients
    Christine M Szych
    Department of Pathology, University of Rochester, Strong Memorial Hospital, 601 Elmwood Avenue, P O Box 704, Rochester, NY 14642, USA
    Cancer Genet Cytogenet 174:132-7. 2007

Collaborators

  • Nancy Wang
  • Christine M Szych
  • M Anwar Iqbal
  • Angham Al-Mutair
  • Jane L Liesveld
  • Liqiong Li
  • Susan Siebert
  • Adam Lee
  • Courtney Asmus
  • Tarekh Owaidah
  • Hamad M Al-Omar
  • Hind Al-Humaidan
  • Zahirul A Bhuiyan
  • Entezam Sahovic
  • Nadia Sakati
  • Abdullah Ashwal

Detail Information

Publications5

  1. ncbi request reprint Complex de novo cryptic subtelomeric rearrangements in a fetus with multiple ultrasonographic abnormalities and a normal karyotype at amniocentesis
    M Anwar Iqbal
    Section of Cytogenetics Molecular Genetics, Department of Pathology and Laboratory Medicine, King Faisal Specialist Hospital and Research Center, Riyadh, Kingdom of Saudi Arabia
    Prenat Diagn 25:1142-9. 2005
    ..We wanted to detect cryptic subtelomeric rearrangements (CSTR) in a fetus with multiple abnormal ultrasonographic findings that revealed a normal karyotype at amniocentesis...
  2. ncbi request reprint del(6)(p23) in two cases of de novo AML--a new recurrent primary chromosome abnormality
    M Anwar Iqbal
    Section of Cytogenetics Molecular Genetics, Department of Pathology and Laboratory Medicine, King Faisal Cancer Center, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia
    Eur J Haematol 77:245-50. 2006
    ..In this report, we present two young adult patients with de novo AML-M2 and a terminal deletion 6p23 as a sole primary abnormality, confirmed by chromosome 6 specific subtelomeric probes...
  3. ncbi request reprint Interstitial del(20)(q11.2q12) - clinical and molecular cytogenetic characterization
    M Anwar Iqbal
    Cytogenetics and Molecular Cytogenetics, Department of Pathology and Laboratory Medicine, Saudi Arabia
    Am J Med Genet A 143:1880-4. 2007
    ..2q12) by high-resolution microarray comparative genomic hybridization (arrayCGH) showed an approximately 6.8 Mb deletion. To our knowledge this is the first report of a de novo interstitial del(20)(q11.2q12) characterized by arrayCGH...
  4. ncbi request reprint Cytogenetics and etiology of ambiguous genitalia in 120 pediatric patients
    Angham Al-Mutair
    Department of Pediatrics, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia
    Ann Saudi Med 24:368-72. 2004
    ..Sex assignment in these children continues to be a challenging diagnostic and therapeutic problem. We studied the causes and characteristics of ambiguous genitalia in children who were referred to a cytogenetic laboratory...
  5. ncbi request reprint Isodicentric Philadelphia chromosomes in imatinib mesylate (Gleevec)-resistant patients
    Christine M Szych
    Department of Pathology, University of Rochester, Strong Memorial Hospital, 601 Elmwood Avenue, P O Box 704, Rochester, NY 14642, USA
    Cancer Genet Cytogenet 174:132-7. 2007
    ..The impact of the isodicentric Philadelphia chromosomes on genomic instability, heterogeneity, and amplification of the Philadelphia chromosomes in IM-resistant patients is discussed...