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  2. Triploid syndrome - Wikipedia

    en.wikipedia.org/wiki/Triploid_syndrome

    Triploid syndrome, also called triploidy, is a chromosomal disorder in which a fetus has three copies of every chromosome instead of the normal two. If this occurs in only some cells, it is called mosaic triploidy and is less severe. Most embryos with triploidy miscarry early in development.

  3. Polyploidy - Wikipedia

    en.wikipedia.org/wiki/Polyploidy

    Polyploidy is a condition in which the cells of an organism have more than two paired sets of chromosomes. Most species whose cells have nuclei ( eukaryotes ) are diploid , meaning they have two complete sets of chromosomes, one from each of two parents; each set contains the same number of chromosomes, and the chromosomes are joined in pairs ...

  4. Diploid-triploid mosaicism - Wikipedia

    en.wikipedia.org/wiki/Diploid-triploid_mosaicism

    Diploid-triploid mosaicism is a human chromosome disorder. Individuals with diploid-triploid syndrome have some cells with three copies of each chromosome for a total of 69 chromosomes (called triploid cells) and some cells with the usual 2 copies of each chromosome for a total of 46 chromosomes (called diploid cells). [1]

  5. Ploidy - Wikipedia

    en.wikipedia.org/wiki/Ploidy

    Triploid organisms, for instance, are usually sterile. Because of this, triploidy is commonly exploited in agriculture to produce seedless fruit such as bananas and watermelons. If the fertilization of human gametes results in three sets of chromosomes, the condition is called triploid syndrome. [citation needed]

  6. Molar pregnancy - Wikipedia

    en.wikipedia.org/wiki/Molar_pregnancy

    Most partial moles are triploid (three chromosome sets). The nucleus contains one maternal set of genes and two paternal sets. The mechanism is usually the reduplication of the paternal haploid set from a single sperm, but may also be the consequence of dispermic (two sperm) fertilization of the egg. [10]

  7. Human genome - Wikipedia

    en.wikipedia.org/wiki/Human_genome

    The human genome is a complete set of nucleic acid sequences for humans, encoded as the DNA within each of the 24 distinct chromosomes in the cell nucleus. A small DNA molecule is found within individual mitochondria. These are usually treated separately as the nuclear genome and the mitochondrial genome. [1]

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  9. Fertilisation - Wikipedia

    en.wikipedia.org/wiki/Fertilisation

    The nucleus of the other sperm cell fuses with two haploid polar nuclei (contained in the central cell) in the centre of the gametophyte. The resulting cell is triploid (3n). This triploid cell divides through mitosis and forms the endosperm, a nutrient-rich tissue, inside the seed. [7]