Muhammad Faiyaz-Ul-Haque

Muhammad Faiyaz-Ul-Haque

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Muhammad Faiyaz-Ul-Haque

Muhammad Faiyaz-Ul-Haque

Publications by authors named "Muhammad Faiyaz-Ul-Haque"

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Mutations in MSX1, PAX9 and MMP20 genes in Saudi Arabian patients with tooth agenesis.

Eur J Med Genet 2016 Aug 27;59(8):377-85. Epub 2016 Jun 27.

Food and Nutrition, Commonwealth Scientific and Industrial Research Organization (CSIRO), Gate 13, Kintore Avenue, Adelaide, 5000 Australia. Electronic address:

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http://dx.doi.org/10.1016/j.ejmg.2016.06.004DOI Listing
August 2016

Recurrent mutation in CDMP1 in a family with Grebe chondrodysplasia: broadening the phenotypic manifestation of syndrome in Pakistani population.

Pak J Med Sci 2015 Nov-Dec;31(6):1542-4

Sajid Malik, Human Genetics Program, Department of Animal Sciences, Faculty of Biological Sciences, Quaid-i-Azam University, 45320 Islamabad, Pakistan.

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http://pjms.com.pk/index.php/pjms/article/view/8115
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http://dx.doi.org/10.12669/pjms.316.8115DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4744317PMC
February 2016

Clinical, neuroimaging, and genetic features of L-2-hydroxyglutaric aciduria in Arab kindreds.

Ann Saudi Med 2014 Mar-Apr;34(2):107-14

Dr. Muhammad Faiyaz-Ul-Haque, Department of Pathology,, College of Medicine,, King Khaled University Hospital,, King Saud University, T: 966-11-4699377, F: +966-11-4672462,

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http://dx.doi.org/10.5144/0256-4947.2014.107DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6074860PMC
November 2015

Autoimmune polyglandular syndrome type 1 in Saudi children.

Saudi Med J 2010 Jul;31(7):788-92

Section of Pediatric Endocrinology, Department of Pediatrics, MBC 58, King Faisal Specialist Hospital and Research Center, PO Box 3354, Riyadh 11211, Kingdom of Saudi Arabia.

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July 2010

A novel HAX1 gene mutation in severe congenital neutropenia (SCN) associated with neurological manifestations.

Eur J Pediatr 2010 Jun 25;169(6):661-6. Epub 2010 Feb 25.

Department of Pathology and Laboratory Medicine, Molecular Genetics Laboratory, King Faisal Specialist Hospital & Research Centre, PO Box 3354, MBC#10, Riyadh 11211, Saudi Arabia.

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http://dx.doi.org/10.1007/s00431-010-1150-6DOI Listing
June 2010

Novel and recurrent mutations in the C1NH gene of Arab patients affected with hereditary angioedema.

Int Arch Allergy Immunol 2010 15;151(2):149-54. Epub 2009 Sep 15.

Molecular Genetics Laboratory, Department of Pathology and Laboratory Medicine, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia.

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http://dx.doi.org/10.1159/000236005DOI Listing
February 2010

Novel FBP1 gene mutations in Arab patients with fructose-1,6-bisphosphatase deficiency.

Eur J Pediatr 2009 Dec 4;168(12):1467-71. Epub 2009 Mar 4.

Department of Pathology, Molecular Genetics Laboratory, King Faisal Specialist Hospital & Research Centre, Riyadh 11211, Saudi Arabia.

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http://dx.doi.org/10.1007/s00431-009-0953-9DOI Listing
December 2009

A novel non-sense mutation in the SLC2A10 gene of an arterial tortuosity syndrome patient of Kurdish origin.

Eur J Pediatr 2009 Jul 26;168(7):867-70. Epub 2008 Sep 26.

Division of Cardiology, Department of Medicine, University Health Network & University of Toronto, Toronto, ON, Canada.

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http://dx.doi.org/10.1007/s00431-008-0839-2DOI Listing
July 2009

Grebe-type chondrodysplasia: a novel missense mutation in a conserved cysteine of the growth differentiation factor 5.

J Bone Miner Metab 2008 1;26(6):648-52. Epub 2008 Nov 1.

Molecular Genetics Laboratory, Department of Pathology & Laboratory Medicine, King Faisal Specialist Hospital & Research Centre, P.O. Box 3354, MBC #10, Riyadh, 11211, Riyadh, Saudi Arabia.

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http://dx.doi.org/10.1007/s00774-008-0853-5DOI Listing
December 2008

Profound biotinidase deficiency in a child with predominantly spinal cord disease.

J Child Neurol 2008 Sep 21;23(9):1043-8. Epub 2008 Jul 21.

Sections of Pediatric Neurology, King Faisal Specialist Hospital & Research Center, Riyadh, Saudi Arabia.

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http://dx.doi.org/10.1177/0883073808318062DOI Listing
September 2008

A novel missense mutation in the galactosyltransferase-I (B4GALT7) gene in a family exhibiting facioskeletal anomalies and Ehlers-Danlos syndrome resembling the progeroid type.

Am J Med Genet A 2004 Jul;128A(1):39-45

Program in Genetics and Genomic Biology, Department of Genetics, The Hospital for Sick Children, 9th Floor Elm Wing, Rm. 9115, 555 University Avenue, Toronto, Ontario M5G 1X8, Canada.

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http://doi.wiley.com/10.1002/ajmg.a.30005
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http://dx.doi.org/10.1002/ajmg.a.30005DOI Listing
July 2004

A new type of Ehlers-Danlos syndrome associated with tortuous systemic arteries in a large kindred from Qatar.

Acta Paediatr 2003 Apr;92(4):456-62

Department of Pediatrics, Hamad Medical Corporation, Doha, Qatar.

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http://dx.doi.org/10.1111/j.1651-2227.2003.tb00578.xDOI Listing
April 2003