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Related Concept Videos

Case Studies01:22

Case Studies

There are many research methods available to psychologists in their efforts to understand, describe, and explain behavior and the cognitive and biological processes that underlie it.
Crossing Over01:34

Crossing Over

Unlike mitosis, meiosis aims for genetic diversity in its creation of haploid gametes. Dividing germ cells first begin this process in prophase I, where each chromosome—replicated in S phase—is now composed of two sister chromatids (identical copies) joined centrally.
The homologous pairs of sister chromosomes—one from the maternal and one from the paternal genome—then begin to align alongside each other lengthwise, matching corresponding DNA positions in a process called synapsis.
In order to...
Crossing Over01:30

Crossing Over

Crossing over is the exchange of genetic information between homologous chromosomes during prophase I of meiosis I. Genetic recombination gives rise to allelic diversity in the newly formed daughter cells. In humans, crossing over produces genetically distinct haploid egg and sperm cells that undergo fertilization to produce unique offspring. Before cell division starts, the germ cell’s chromosome(s) undergo duplication in the S phase of the cell cycle. As the cells enter prophase I, duplicated...
Sutures of the Skull01:22

Sutures of the Skull

The human skull is composed of several bones that come together to protect the brain and support the structures of the face. The junctions where these bones meet are called sutures.
Sutures are immobile joints between adjacent bones of the skull. The narrow gap between the bones is filled with dense, fibrous connective tissue that unites the bones. The long sutures located between the skull bones are not straight but instead follow irregular, tightly twisting paths. These twisting lines tightly...
Nondisjunction01:29

Nondisjunction

During meiosis, chromosomes occasionally separate improperly. This occurs due to failure of homologous chromosome separation during meiosis I or failed sister chromatid separation during meiosis II. In some species, notably plants, nondisjunction can result in an organism with an entire additional set of chromosomes, which is called polyploidy. In humans, nondisjunction can occur during male or female gametogenesis and the resulting gametes possess one too many or one too few chromosomes.
Nondisjunction01:29

Nondisjunction

During meiosis, chromosomes occasionally separate improperly. This occurs due to failure of homologous chromosome separation during meiosis I or failed sister chromatid separation during meiosis II. In some species, notably plants, nondisjunction can result in an organism with an entire additional set of chromosomes, which is called polyploidy. In humans, nondisjunction can occur during male or female gametogenesis and the resulting gametes possess one too many or one too few chromosomes.

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Related Experiment Video

Updated: Jun 17, 2026

Model Surgical Training: Skills Acquisition in Fetoscopic Laser Photocoagulation of Monochorionic Diamniotic Twin Placenta Using Realistic Simulators
09:51

Model Surgical Training: Skills Acquisition in Fetoscopic Laser Photocoagulation of Monochorionic Diamniotic Twin Placenta Using Realistic Simulators

Published on: March 21, 2018

[Conjoined twins. Historical review].

Valgardur Egilsson, Hannes Petersen

    Laeknabladid
    |December 10, 2009
    PubMed
    Summary

    This study reviews Icelandic historical logs, identifying five cases of conjoined twinning. It proposes a new view of the pathogenesis of this rare newborn malformation.

    Area of Science:

    • Embryology and teratology
    • Medical history
    • Perinatal medicine

    Context:

    • Conjoined twinning is a rare congenital anomaly with significant implications for newborn health.
    • Historical medical records offer unique insights into the prevalence and understanding of congenital malformations.
    • Icelandic historical logs provide a specific, underutilized resource for studying rare medical phenomena.

    Purpose:

    • To investigate the historical documentation of conjoined twinning in Iceland.
    • To analyze the embryologic background and propose novel insights into the pathogenesis of conjoined twinning.
    • To contribute to the understanding of rare congenital malformations through historical data.

    Summary:

    • The study examines Icelandic historical logs, identifying four definite and one uncertain case of conjoined twinning.

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    Accurate and Simple Evaluation of Vascular Anastomoses in Monochorionic Placenta using Colored Dye
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    Accurate and Simple Evaluation of Vascular Anastomoses in Monochorionic Placenta using Colored Dye

    Published on: September 5, 2011

    Related Experiment Videos

    Last Updated: Jun 17, 2026

    Model Surgical Training: Skills Acquisition in Fetoscopic Laser Photocoagulation of Monochorionic Diamniotic Twin Placenta Using Realistic Simulators
    09:51

    Model Surgical Training: Skills Acquisition in Fetoscopic Laser Photocoagulation of Monochorionic Diamniotic Twin Placenta Using Realistic Simulators

    Published on: March 21, 2018

    Guide Wire Assisted Catheterization and Colored Dye Injection for Vascular Mapping of Monochorionic Twin Placentas
    09:04

    Guide Wire Assisted Catheterization and Colored Dye Injection for Vascular Mapping of Monochorionic Twin Placentas

    Published on: September 5, 2011

    Accurate and Simple Evaluation of Vascular Anastomoses in Monochorionic Placenta using Colored Dye
    09:52

    Accurate and Simple Evaluation of Vascular Anastomoses in Monochorionic Placenta using Colored Dye

    Published on: September 5, 2011

  • It provides an overview of the embryologic origins of conjoined twinning.
  • New perspectives on the pathogenesis of conjoined twinning are presented based on historical and embryological data.
  • Impact:

    • Enhances understanding of the historical prevalence of conjoined twinning in a specific population.
    • Offers a novel theoretical framework for the pathogenesis of conjoined twinning.
    • Highlights the value of historical archives in medical research, particularly for rare conditions.