An analysis of the distribution of hetero- and isodisomic regions of chromosome 7 in five mUPD7 Silver-Russell syndrome probands
S N Abu-Amero , P Stanier , K K Abu-Amero , M A Preece
Journal of Medical Genetics 36 ( 6) 457 -460
54
1999
Status of antituberculosis drug resistance in Saudi Arabia 1979-98.
K K Abu-Amero
Eastern Mediterranean Health Journal 8 664 -670
17
2002
Association of mitochondrial DNA transversion mutations with familial medullary thyroid carcinoma/multiple endocrine neoplasia type 2 syndrome.
K K Abu-Amero , A S Alzahrani , M Zou , Y Shi
Oncogene 25 ( 5) 677 -684
45
2006
Increased relative mitochondrial DNA content in leucocytes of patients with NAION.
K K Abu-Amero , T M Bosley
British Journal of Ophthalmology 90 ( 7) 823 -825
20
2006
Nisin resistance distinguishes Mycoplasma spp. from Acholeplasma spp. and provides a basis for selective growth media.
K K Abu-Amero , M A Halablab , R J Miles
Applied and Environmental Microbiology 62 ( 9) 3107 -3111
7
1996
GSTM1 and GSTT1 deletion genotypes in various spontaneous optic neuropathies in Arabs.
K K Abu-Amero , B Milcarek , T M Bosley
British Journal of Ophthalmology 93 ( 8) 1101 -1104
11
2009
Overview of the laboratory accreditation programme of the College of American Pathologists.
Abu-Amero Kk
Eastern Mediterranean Health Journal 8 654 -663
7
2002
Evaluation of the COBAS AMPLICOR MTB test for the detection of Mycobacterium tuberculosis complex.
Halablab Ma , Abu-Amero Kk
Eastern Mediterranean Health Journal 10 ( 3) 329
2
2004
Mitochondrial DNA abnormalities in NAION.
K. K Abu-Amero , T. M Bosley
British Journal of Ophthalmology 91 ( 11) 1561 -1561
5
2007
Ophthalmic genetics: Moving forward
KhaledK Abu-Amero
Middle East African Journal of Ophthalmology 18 ( 1) 1 -1
2011
Leber's Hereditary Optic Neuropathy: The Mitochondrial Connection Revisited.
KhaledK Abu-Amero
Middle East African Journal of Ophthalmology 18 ( 1) 17 -23
12
2011
Severe type I protein C deficiency with neonatal purpura fulminans due to a novel homozygous mutation in exon 6 of the protein C gene.
K. K. ABU-AMERO , T. M. OWAIDAH , M. AL-MAHED
Journal of Thrombosis and Haemostasis 4 ( 5) 1152 -1153
5
2006
Spectrum of factor VIII mutations in Arab patients with severe haemophilia A.
K. K. ABU-AMERO , A. HELLANI , M. AL-MAHED , I. AL-SHEIKH
Haemophilia 14 ( 3) 484 -488
15
2008
Neurologic Features of Genetically Defined Lipoid Proteinosis
Khaled Abu Amero , S AlRashid , I Al Orainy , D Oystreck
JOURNAL OF MEDICAL GENETICS 47 S85 -S85
2010
A de novo Marker Chromosome derived from 9p in a Patient with Autism Genotype-Phenotype Correlation
Khaled Abu Amero , A Helani , M Salih , M Seidahmed
JOURNAL OF MEDICAL GENETICS 47 S99 -S99
2010
Keratoconus: globally and in the middle east (epidemiology, genetics, and future research)
Ahmed Mousa , Altaf Kondkar , Khaled K Abu Amero
Advances in Vision Research, Volume I: Genetic Eye Research in Asia and the Pacific 391 -402
3
2017
27 Keratoconus: Globally and in the Middle East (Epidemiology, Genetics, and Future Research)
Ahmed Mousa , Altaf Kondkar , Khaled K Abu Amero
Advances in Vision Research, Volume I: Genetic Eye Research in Asia and the Pacific 391 -391
2017
Bibliography Current World Literature Vol 18 No 2 March 2007
KK Abu Amero , J Morales , TM Bosley , OA Agapova
pathogenesis 47 2508 -2514
2006
Molecular Genetics Laboratory: Detailed Requirements for Accreditation by the College of American Pathologists
Khaled Khader Abu-Amero , Sayeda Nasreen Abu-Amero , Sayeda Nasreen Abu-Amero22
Molecular Biology Today 2 ( 3) 45 -59
2001
Biochemical characterization of acholeplasma and mycoplasma and their interaction with liposomes.
Khaled Khader Salem Abu-Amero
King's College London (University of London)
1997