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Translations:Erbkrankheiten/2/en: Unterschied zwischen den Versionen

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Every human carries two copies of each gene in his chromosomes = alleles. Each allele comes from one parent. Hereditary diseases that occur within families are the result of a [[mutation]] in a single gene and follow a predictable inheritance. In other words, the disease already occurred in the ancestors of this family, a phenomenon that can be observed in the family tree. Inheritance can take place in the following ways:
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Every human carries two copies of each gene in his chromosomes = alleles. Each allele comes from one parent. Hereditary diseases that occur within families are the result of a [[Mutation/en|mutation]] in a single gene and follow a predictable inheritance. In other words, the disease already occurred in the ancestors of this family, a phenomenon that can be observed in the family tree. Inheritance can take place in the following ways:

Aktuelle Version vom 22. Mai 2019, 00:24 Uhr

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Nachricht im Original (Erbkrankheiten)
Jeder Mensch trägt in seinen Chromosomen von jedem Gen zwei Kopien = Allele. Jeweils ein Allel stammt von einem Elternteil. Erbkrankheiten, die innerhalb von Familien auftreten, sind die Folge einer [[Mutation]] in einem einzigen Gen und folgen einem vorhersehbaren Erbgang. Mit anderen Worten: Die Krankheit trat in dieser Familie bereits bei den Vorfahren auf, ein Phänomen, das im Stammbaum beobachtet werden kann. Die Vererbung kann auf folgende Weisen erfolgen:
ÜbersetzungEvery human carries two copies of each gene in his chromosomes = alleles. Each allele comes from one parent. Hereditary diseases that occur within families are the result of a [[Mutation/en|mutation]] in a single gene and follow a predictable inheritance. In other words, the disease already occurred in the ancestors of this family, a phenomenon that can be observed in the family tree. Inheritance can take place in the following ways:

Every human carries two copies of each gene in his chromosomes = alleles. Each allele comes from one parent. Hereditary diseases that occur within families are the result of a mutation in a single gene and follow a predictable inheritance. In other words, the disease already occurred in the ancestors of this family, a phenomenon that can be observed in the family tree. Inheritance can take place in the following ways: