Mara Giordano
0000-0001-6686-4600
76 papers found
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Molecular analysis of the growth hormone releasing hormone receptor gene (GHRH-R) in isolated growth hormone deficiency: Identification of a likely etiological mutation in the signal peptide
Molecular Analysis of the Growth Hormone Gene (GH1) in Isolated Growth Hormone Deficiency
Determination of SNP allele frequencies in pooled DNAs by primer extension genotyping and denaturing high-performance liquid chromatography
Study of Two Ectopeptidases in the Susceptibility to Celiac Disease: Two Newly Identified Polymorphisms of Dipeptidylpeptidase IV:
Rapid method for detection of extra (TA) in the promoter of the bilirubin-UDP-glucuronosyl transferase 1 gene associated with Gilbert syndrome
New polymorphisms in the IL-10 promoter region
Linkage disequilibrium between intra-locus variants in the aminopeptidase n gene and test of their association with coeliac disease
Identification by Denaturing High-Performance Liquid Chromatography of Numerous Polymorphisms in a Candidate Region for Multiple Sclerosis Susceptibility
Evidence for gene conversion in the generation of extensive polymorphism in the promoter of the growth hormone gene
Reassessment of the specificity of lens opacities in myotonic dystrophy.
Homozygous tandem duplication within the gene encoding the β-subunit of rod phosphodiesterase as a cause for autosomal recessive retinitis pigmentosa
Problems arising in correlating clinical and molecular data in myotonic dystrophy.
HLA supratypes in an Italian population
Influence of ancestral gender on transmission of familial amyotrophic lateral sclerosis.
Origin of a regressed myotonic dystrophy allele
Gametic association of HSP70-1 promoter region alleles and their inclusion in extended HLA haplotypes
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