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Preimplantation Genetic Diagnosis (CROSBI ID 308794)

Prilog u časopisu | pregledni rad (znanstveni) | međunarodna recenzija

Markova-Car, Elitza ; Pavelić, Krešimir Preimplantation Genetic Diagnosis // Donald School Journal of Ultrasound in Obstetrics and Gynecology, 16 (2022), 1; 79-82. doi: 10.5005/jp-journals-10009-1920

Podaci o odgovornosti

Markova-Car, Elitza ; Pavelić, Krešimir

engleski

Preimplantation Genetic Diagnosis

Preimplantation genetic diagnosis (PGD) or preimplantation genetic screening (PGS) is an early form of prenatal diagnosis which allows that, before the pregnancy has begun, embryos can be tested for genetic disorders. The rationale behind the method lies in the removal of cells from early embryos and genetic analysis of these cells before being transferred to the uterus. This procedure offers an advantage for those couples having genetic disorders whose offspring has an increased risk of a specific genetic condition by helping in the delivery of a healthy baby or prevention of repeated spontaneous abortions. As a result, PGS has developed as a valuable tool for enhancing pregnancy success with assisted reproductive technologies. In fact, PGD may possibly be suggested for any disorder for which molecular testing can be performed.

Embryo, Microarray, Next generation sequencing, Preimplantation genetic diagnosis

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Podaci o izdanju

16 (1)

2022.

79-82

objavljeno

0973-614X

0975-1912

10.5005/jp-journals-10009-1920

Povezanost rada

Kliničke medicinske znanosti, Temeljne medicinske znanosti

Poveznice
Indeksiranost