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autosomal inheritance

См. также в других словарях:

  • autosomal inheritance — autosomal inheritance. См. аутосомное наследование. (Источник: «Англо русский толковый словарь генетических терминов». Арефьев В.А., Лисовенко Л.А., Москва: Изд во ВНИРО, 1995 г.) …   Молекулярная биология и генетика. Толковый словарь.

  • Inheritance — Not something that is contained in a will, but rather a gene, chromosome or genome that is transmitted from parent to child. The pattern of inheritance is the manner in which a gene is transmitted. For example, the pattern of inheritance may be… …   Medical dictionary

  • Autosomal — Pertaining to a chromosome that is not a sex chromosome; relating to any one of the chromosomes save the sex chromosomes. People normally have 22 pairs of autosomes (44 autosomes) in each cell together with two sex chromosomes (X and Y in the… …   Medical dictionary

  • Inheritance, mendelian — The manner in which genes and traits are passed from parents to their children. The four modes of Mendelian inheritance are autosomal dominant, autosomal recessive, X linked dominant and X linked recessive. The term mendelian refers to the great… …   Medical dictionary

  • autosomal dominant hypophosphatemic rickets — (ADHR), autosomal dominant vitamin D–resistant rickets a form of familial hypophosphatemic rickets with autosomal dominant inheritance and caused by mutation in the FGF23 gene (locus: 12p13.3), which encodes a member of the fibroblast growth… …   Medical dictionary

  • pseudoautosomal inheritance — inheritance of traits controlled by genes located in the pseudoautosomal regions of the sex chromosomes and mimicking the patterns of inheritance seen with autosomal genes …   Medical dictionary

  • Online Mendelian Inheritance in Man — (OMIM) is a database that catalogues all the known diseases with a genetic component, and when possible links them to the relevant genes in the human genome and provides references for further research and tools for genomic analysis of a… …   Wikipedia

  • Mendelian Inheritance in Man — The Mendelian Inheritance in Man project is a database that catalogues all the known diseases with a genetic component, and when possible links them to the relevant genes in the human genome and provides references for further research and tools… …   Wikipedia

  • Mendelian inheritance — The manner in which genes and traits are passed from parents to their children. The four modes of Mendelian inheritance are autosomal dominant, autosomal recessive, X linked dominant and X linked recessive. The term mendelian refers to the great… …   Medical dictionary

  • аутосомное наследование — autosomal inheritance аутосомное наследование. Hезависимое от пола (не сцепленное с полом) наследование какого либо признака. (Источник: «Англо русский толковый словарь генетических терминов». Арефьев В.А., Лисовенко Л.А., Москва: Изд во ВНИРО,… …   Молекулярная биология и генетика. Толковый словарь.

  • Tietz syndrome — Not to be confused with Tietze syndrome. Tietz syndrome Classification and external resources ICD 10 E70.3 (ILDS E70.358) OMIM 103500 …   Wikipedia

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