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Showing 1 to 2 of 2 for “"유전질환"”.

  1. Molecular Genetic Analysis of Tumor Cells and Developmenet of RNA Interferance Therpy in Neurofibromatosis Type1(NF1)

    Neurofibromatosis 1 (NF1) is the most common familial cancer syndrome in humans, with a birth incidence of 1:3500 and a prevalence of 1:4000-.1:5000 in the general population. NF1 is transmitted in an autosomal dominant manner, with about 30-50% of NF1 patients representing de novo germline …

    ajou Repository record for Molecular Genetic Analysis of Tumor Cells and Developmenet of RNA Interferance Therpy in Neurofibromatosis Type1(NF1) (opens in a new tab)

  2. A Study of Guideline for Genetic Counselling in Preimplantation Genetic Diagnosis (PGD)

    Preimplantation genetic diagnosis (PGD), also known as embryo screening, is a technique used to identify genetic defects in embryos created through in vitro fertilization before pregnancy. PGD is considered another way to prenatal diagnosis. PGD refers specifically to when one or both genetic …

    ajou Repository record for A Study of Guideline for Genetic Counselling in Preimplantation Genetic Diagnosis (PGD) (opens in a new tab)