Human Genetics HB

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A review of vocabulary associated with Human Genetics.

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human genetics

Edad recomendada: 14 años

33 veces realizada

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Mary Chambers

Estados Unidos

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Crucigrama Human Genetics HBVersión en línea A review of vocabulary associated with Human Genetics. por Mary Chambers 1 The scientific name for the the insect that is commonly used for genetic studies. 2 When researchers select a small sample of a population to represent a larger population. 3 The failure of chromatids to separate during meiosis. 4 A procedure that is used to check the genes of a fetus by removing some of the baby's skin cells in order to do a karyotype. 5 A type of chromosomal mutation where part of a chromosome breaks off and attaches to a non-homologous chromosome. 6 When a single gene can affect multiple phenotypic outcomes. 7 Molecules that are produced by the immune system and defend against specific antigens. 8 This type of mutation shifts the reading frame for the codons because a base is added or deleted. 9 A stage of precancerous cells where the cells are multiplying out of control and look abnormal. 10 Chromosomes found in the human body that do not determine sex. 11 A type of chromosomal mutation where part of a chromosome breaks off and reattaches upside down. 12 A type of trait where it is only found on the X chromosome, but not the Y. 13 A process where chromosomes are matched up with their homologues and placed in order from largest to smallest to see if there are any extra or missing chromosomes. 14 A trait that is controlled by more than two genes. 15 The type of twins that occur when two eggs are fertilized by two sperm at the same time. 16 A type of mutation that occurs in the sex cells. 17 Markers on a cell's surface that identify the cell as native to the body. 18 Any change in the DNA. 19 A family record that shows how a trait is inherited over several generations. 20 A type of point mutation where the protein is not completed because a stop codon is coded for in the middle of the process. 21 Term used to describe people who have one copy of a recessive allele, but do not exhibit the trait. 22 A type of point mutation where the correct amino acid is still coded for. 23 When cells are invading out of control and are invading nearby tissue. 24 A type of mutation that does not progress past the zygote stage. 24 10 5 8 19 23 22 6 12 9 2 21 17 13 1 7 16 11 3 20 4 18 14 15

Crucigrama

Human Genetics HBVersión en línea

A review of vocabulary associated with Human Genetics.

por Mary Chambers

The scientific name for the the insect that is commonly used for genetic studies.

When researchers select a small sample of a population to represent a larger population.

The failure of chromatids to separate during meiosis.

A procedure that is used to check the genes of a fetus by removing some of the baby's skin cells in order to do a karyotype.

A type of chromosomal mutation where part of a chromosome breaks off and attaches to a non-homologous chromosome.

When a single gene can affect multiple phenotypic outcomes.

Molecules that are produced by the immune system and defend against specific antigens.

This type of mutation shifts the reading frame for the codons because a base is added or deleted.

A stage of precancerous cells where the cells are multiplying out of control and look abnormal.

Chromosomes found in the human body that do not determine sex.

A type of chromosomal mutation where part of a chromosome breaks off and reattaches upside down.

A type of trait where it is only found on the X chromosome, but not the Y.

A process where chromosomes are matched up with their homologues and placed in order from largest to smallest to see if there are any extra or missing chromosomes.

Human Genetics HB

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Crucigrama

Human Genetics HBVersión en línea

por Mary Chambers

The scientific name for the the insect that is commonly used for genetic studies.

When researchers select a small sample of a population to represent a larger population.

The failure of chromatids to separate during meiosis.

A procedure that is used to check the genes of a fetus by removing some of the baby's skin cells in order to do a karyotype.

A type of chromosomal mutation where part of a chromosome breaks off and attaches to a non-homologous chromosome.

When a single gene can affect multiple phenotypic outcomes.

Molecules that are produced by the immune system and defend against specific antigens.

This type of mutation shifts the reading frame for the codons because a base is added or deleted.

A stage of precancerous cells where the cells are multiplying out of control and look abnormal.

Chromosomes found in the human body that do not determine sex.

A type of chromosomal mutation where part of a chromosome breaks off and reattaches upside down.

A type of trait where it is only found on the X chromosome, but not the Y.

A process where chromosomes are matched up with their homologues and placed in order from largest to smallest to see if there are any extra or missing chromosomes.

A trait that is controlled by more than two genes.

The type of twins that occur when two eggs are fertilized by two sperm at the same time.

A type of mutation that occurs in the sex cells.

Markers on a cell's surface that identify the cell as native to the body.

Any change in the DNA.

A family record that shows how a trait is inherited over several generations.

A type of point mutation where the protein is not completed because a stop codon is coded for in the middle of the process.

Term used to describe people who have one copy of a recessive allele, but do not exhibit the trait.

A type of point mutation where the correct amino acid is still coded for.

When cells are invading out of control and are invading nearby tissue.

A type of mutation that does not progress past the zygote stage.