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- 2001
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Mark
Clinical expressions of juvenile hereditary retinal degenerations and macular dystrophies: Electrophysiological and genetic studies
2001)(
- Thesis › Doctoral thesis (compilation)
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Mark
Novel TFAP2B mutations that cause Char syndrome provide a genotype-phenotype correlation
(
- Contribution to journal › Article
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Mark
Prediction of osteoporotic fractures by bone densitometry and COLIA1 genotyping : a prospective, population-based study in men and women
(
- Contribution to journal › Article
-
Mark
COL1A1 Sp1 polymorphism predicts perimenopausal and early postmenopausal spinal bone loss
(
- Contribution to journal › Article
-
Mark
Effect of a COL1A1 Sp1 binding site polymorphism on arterial pulse wave velocity : an index of compliance
(
- Contribution to journal › Article
-
Mark
The NciI polymorphism in the cyclin D1 gene and sporadic primary hyperparathyroidism
(
- Contribution to journal › Article
- 2000
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Mark
Hyperhomocysteinemia and the MTHFR C677T mutation in central retinal vein occlusion
(
- Contribution to journal › Article
- 1999
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Mark
Prenatal diagnosis of haemophilia
(
- Contribution to journal › Scientific review
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Mark
HLA associations in type 1 diabetes among patients not carrying high-risk DR3-DQ2 or DR4-DQ8 haplotypes
(
- Contribution to journal › Article
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Mark
The prothrombin gene G20210A mutation and the platelet glycoprotein IIIa polymorphism PlA2 in patients with central retinal vein occlusion
(
- Contribution to journal › Article