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Results:
1-9
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Results: 9
Authors:
Martignetti, JA
Al Aqeel, A
Al Sewairi, W
Boumah, CE
Kambouris, M
Al Mayouf, S
Sheth, KV
Al Eid, W
Dowling, O
Harris, J
Glucksman, MJ
Bahabri, S
Meyer, BF
Desnick, RJ
Citation: Ja. Martignetti et al., Mutation of the matrix metalloproteinase 2 gene (MMP2) causes a multicentric osteolysis and arthritis syndrome, NAT GENET, 28(3), 2001, pp. 261-265
Authors:
Kambouris, M
Banjar, H
Moggari, I
Nazer, H
Al-Hamed, M
Meyer, BF
Citation: M. Kambouris et al., Identification of novel mutations in Arabs with cystic fibrosis and their impact on the cystic fibrosis transmembrane regulator mutation detection rate in Arab populations, EUR J PED, 159(5), 2000, pp. 303-309
Authors:
Dzimiri, N
Basco, C
Moorji, A
Meyer, BF
Citation: N. Dzimiri et al., Angiotensin-converting enzyme polymorphism and the risk of coronary heart disease in the Saudi male population, ARCH PATH L, 124(4), 2000, pp. 531-534
Authors:
Kambouris, M
Meyer, BF
Citation: M. Kambouris et Bf. Meyer, Interpretation of linkage data for a Huntington-like disorder mapping to 4p15.3 - Reply, AM J HU GEN, 67(1), 2000, pp. 263-263
Authors:
Kambouris, M
Bohlega, S
Al-Tahan, A
Meyer, BF
Citation: M. Kambouris et al., Localization of the gene for a novel autosomal recessive neurodegenerativeHuntington-like disorder to 4p15.3, AM J HU GEN, 66(2), 2000, pp. 445-452
Authors:
Banjar, H
Kambouris, M
Meyer, BF
Al-Mehaidib, A
Mogarri, I
Citation: H. Banjar et al., Geographic distribution of cystic fibrosis transmembrane regulator gene mutations in Saudi Arabia, ANN TROP PA, 19(1), 1999, pp. 69-73
Authors:
Diaz, GA
Gelb, BD
Ali, F
Sakati, N
Sanjad, S
Meyer, BF
Kambouris, M
Citation: Ga. Diaz et al., Sanjad-sakati and autosomal recessive Kenny-Caffey syndromes are allelic: Evidence for an ancestral founder mutation and locus refinement, AM J MED G, 85(1), 1999, pp. 48-52
Authors:
Al-Jishi, E
Meyer, BF
Rashed, MS
Al-Essa, M
Al-Hamed, MH
Sakati, N
Sanjad, S
Ozand, PT
Kambouris, M
Citation: E. Al-jishi et al., Clinical, biochemical, and molecular characterization of patients with glutathione synthetase deficiency, CLIN GENET, 55(6), 1999, pp. 444-449
Authors:
Dzimiri, N
Meyer, BF
Hussain, SS
Basco, C
Afrane, B
Halees, Z
Citation: N. Dzimiri et al., Relevance of apolipoprotein E polymorphism for coronary artery disease in the Saudi population, ARCH PATH L, 123(12), 1999, pp. 1241-1245
Risultati:
1-9
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