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Genomic Journey's

Genomic Journey's

Written by: Team Genomic Journey's
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The podcast “Genomic Journeys” is a series of discussions on scientific articles related to molecular biology and medical genetics. The project is organized by students of the “Molecular Biology and Medical Genetics” club at the West Kazakhstan Medical University named after M. Ospanov. Through this podcast, students can immerse themselves in the world of science and stay updated on the latest research in the field of genetics and its applications in medicine.

The goal of the project is to promote the reading of scientific articles among university students and to foster their interest in current scientific research and discoveries.

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Episodes
  • Arise of MONGOLIAN SPOTS (русский)

    Arise of MONGOLIAN SPOTS (русский)
    Feb 7 2026

    Описание эпизода 1

    В данном эпизоде мы рассматриваем редкое генетическое состояние на основе научной статьи.

    «Атипичные проявления у новорождённого с дупликацией de novo 17p11.2p13.2: клинический случай»,

    авторы — Shravan Kumar Katam и соавт., опубликованной в журнале Annals of Genetics and Genetic Disorders (ноябрь 2021 г.).

    В статье представлен клинический случай новорождённого с уникальной хромосомной дупликацией. В эпизоде обсуждаются особенности клинической картины и генетические аспекты, имеющие значение для ведения редких врождённых заболеваний.

    Слушатели узнают, каким образом современные достижения в области генетики способствуют диагностике сложных состояний в неонатальной практике и расширяют возможности оказания медицинской помощи новорождённым.

    🔗 Ссылка на статью:

    https://www.remedypublications.com/annals-of-genetics-genetic-disorders-abstract.php?aid=8252
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    6 mins
  • Arise of MONGOLIAN SPOTS

    Arise of MONGOLIAN SPOTS
    Oct 17 2024

    Episode 1 description: In this episode, we explore a rare genetic condition from the article

    “Atypical Features in a Neonate with de novo 17p11.2p13.2 Duplication Syndrome - A Case

    Report” by Shravan Kumar Katam et al., published in the Annals of Genetics and Genetic

    Disorders (November 2021). The case involves a neonate with a unique chromosomal

    duplication. We discuss the clinical presentation and genetic insights for managing rare

    congenital disorders. Tune in to learn how advances in genetics are transforming neonatal care.

    Listeners will gain valuable insights into the role of genetic research in diagnosing complex

    conditions.

    Article link 🔗 https://www.remedypublications.com/annals-of-genetics-genetic-disorders-abstract.php?aid=8252
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    9 mins
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