M Anwar Iqbal

Summary

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

Publications

  1. ncbi request reprint Cytogenetic diagnosis of fragile X syndrome: study of 305 suspected cases in Saudi Arabia
    M A Iqbal
    Department of Pathology, Section of Cytogenetics Molecular Genetics, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia
    Ann Saudi Med 20:214-7. 2000
  2. 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
  3. 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
  4. 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
  5. pmc Renal failure associated with APECED and terminal 4q deletion: evidence of autoimmune nephropathy
    Mohammed Al-Owain
    Department of Medical Genetics, King Faisal Specialist Hospital and Research Centre, Riyadh 11211, Saudi Arabia
    Clin Dev Immunol 2010:586342. 2010
  6. 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
  7. 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

  • Jean Laurent Casanova
  • Namik Kaya
  • Saleh Al-Muhsen
  • Nancy Wang
  • Mohammed Al-Owain
  • Christine M Szych
  • M Anwar Iqbal
  • Angham Al-Mutair
  • Hindi Al-Hindi
  • Hadeel Al-Manea
  • Hamad Al-Mojalli
  • Albandary Al-Bakheet
  • Ibrahim Bin Hussain
  • Anne Puel
  • Hamad Al-Zaidan
  • Shelley Kennedy
  • Susan Siebert
  • Adam Lee
  • Courtney Asmus
  • Liqiong Li
  • Jane L Liesveld
  • Hind Al-Humaidan
  • Zahirul A Bhuiyan
  • Hamad M Al-Omar
  • Entezam Sahovic
  • Tarekh Owaidah
  • Nadia Sakati
  • Abdullah Ashwal

Detail Information

Publications7

  1. ncbi request reprint Cytogenetic diagnosis of fragile X syndrome: study of 305 suspected cases in Saudi Arabia
    M A Iqbal
    Department of Pathology, Section of Cytogenetics Molecular Genetics, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia
    Ann Saudi Med 20:214-7. 2000
    ..4-0.8 per 1000 in males and 0.2-0.6 per 1000 in females. In this study, we have determined the frequency of fragile X-positive cases in 305 preselected patients...
  2. 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...
  3. 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...
  4. 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...
  5. pmc Renal failure associated with APECED and terminal 4q deletion: evidence of autoimmune nephropathy
    Mohammed Al-Owain
    Department of Medical Genetics, King Faisal Specialist Hospital and Research Centre, Riyadh 11211, Saudi Arabia
    Clin Dev Immunol 2010:586342. 2010
    ..This is, to the best of our knowledge, the first paper showing evidence of autoimmune nephropathy by renal immunofluorescence in a patient with APECED and terminal 4q deletion...
  6. 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...
  7. 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...