Read more about the article Ethics of preimplantation diagnosis: recordings from the Fourth International Symposium on Preimplantation Genetics.
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Ethics of preimplantation diagnosis: recordings from the Fourth International Symposium on Preimplantation Genetics.

Abstract New ethical issues emerge from the rapid expansion in knowledge of preimplantation genetics. These were summarized and debated recently during the final session at the Fourth International Symposium on…

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Read more about the article BRCA2 germline mutations in Cypriot patients with familial breast/ovarian cancer.
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BRCA2 germline mutations in Cypriot patients with familial breast/ovarian cancer.

Abstract Germline mutations in the BRCA2 gene have been shown to be associated with familial female and male breast cancer. Mutations occur throughout the entire coding region of the gene,…

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Read more about the article Spectrum and prevalence of prothrombotic single nucleotide polymorphism profiles in the Greek Cypriot population.
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Spectrum and prevalence of prothrombotic single nucleotide polymorphism profiles in the Greek Cypriot population.

Abstract This study was performed to establish the allele, genotype and genotype combination/SNP (single nucleotide polymorphism) profile frequencies in the general population of Cyprus for 6 genes implicated in thrombotic…

Continue ReadingSpectrum and prevalence of prothrombotic single nucleotide polymorphism profiles in the Greek Cypriot population.
Read more about the article Abstracts of the 4th International Symposium on Preimplantation Genetics. Limassol, Cyprus, 10-13 April 2002.
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Abstracts of the 4th International Symposium on Preimplantation Genetics. Limassol, Cyprus, 10-13 April 2002.

Abstract

Continue ReadingAbstracts of the 4th International Symposium on Preimplantation Genetics. Limassol, Cyprus, 10-13 April 2002.
Read more about the article A novel NF-L mutation Pro22Ser is associated with CMT2 in a large Slovenian family.
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A novel NF-L mutation Pro22Ser is associated with CMT2 in a large Slovenian family.

Abstract Charcot-Marie-Tooth (CMT) disease is the most-common form of inherited motor and sensory neuropathy. The autosomal dominant axonal form of the disease (CMT2) is currently subdivided into seven types based…

Continue ReadingA novel NF-L mutation Pro22Ser is associated with CMT2 in a large Slovenian family.
Read more about the article DNazyme-mediated cleavage of Twist transcripts and increase in cellular apoptosis.
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DNazyme-mediated cleavage of Twist transcripts and increase in cellular apoptosis.

Abstract DNazymes is a group of catalytic nucleic acids that can be designed to cleave target mRNA molecules in a base-specific way. Twist is a basic helix-loop-helix transcription factor that…

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Read more about the article Phylogeographical variation of chloroplast DNA in holm oak (Quercus ilex L.).
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Phylogeographical variation of chloroplast DNA in holm oak (Quercus ilex L.).

Abstract Variation in the lengths of restriction fragments (RFLPs) of the whole chloroplast DNA molecule was studied in 174 populations of Quercus ilex L. sampled over the entire distribution of…

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Read more about the article Effects of transmission of Y chromosome AZFc deletions.
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Effects of transmission of Y chromosome AZFc deletions.

Abstract Deletions of specific regions on the Y chromosome cause male infertility. Recent advances in infertility treatment allow Y chromosome deletions to be transmitted to male offspring with the assumption…

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Read more about the article Autosomal-dominant medullary cystic kidney disease type 1: clinical and molecular findings in six large Cypriot families.
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Autosomal-dominant medullary cystic kidney disease type 1: clinical and molecular findings in six large Cypriot families.

Abstract Autosomal-dominant medullary cystic kidney disease (ADMCKD), a hereditary chronic interstitial nephropathy, recently attracted attention because of the cloning or mapping of certain gene loci, namely NPHP1, NPHP2 and NPHP3…

Continue ReadingAutosomal-dominant medullary cystic kidney disease type 1: clinical and molecular findings in six large Cypriot families.