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Vertaling van "Cytoplasmic inheritance " (Engels → Nederlands) :

cytoplasmic heredity | cytoplasmic inheritance | extra-nuclear inheritance | plasmatic heredity

http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]

cytoplasmatische overerving | extra nucleaire overerving

http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]

http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]

abnormality of the cytoplasm | anomaly of the cytoplasm | cytoplasmic abnormality

http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]

anomalie van het cytoplasma

http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]

http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]

Hereditary mixed polyposis syndrome (HMPS) describes an autosomal dominantly inherited large-bowel disease with characteristics of the presence of a mixture of hyperplastic, atypical juvenile and adenomatous polyps that are associated with an increas

https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]

hereditary mixed polyposis syndrome

https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]

https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]

Morvan's disease Nelaton's syndrome Sensory neuropathy:dominantly inherited | recessively inherited

https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]

https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]

https://terminologie.nictiz.nl (...) [HTML] [2018-01-01]

inheritance law | law of inheritance | law of succession | law on succession

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erfrecht

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http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]

birth right council practices | inheritance council | heritage council practices | inheritance council practices

https://ec.europa.eu/esco/port (...) (...) [HTML] [2017-12-31]

praktijken van de erfgoedraad

https://ec.europa.eu/esco/port (...) (...) [HTML] [2017-12-31]

https://ec.europa.eu/esco/port (...) [HTML] [2017-12-31]

A rare genetic axonal peripheral sensorimotor neuropathy with an X-linked recessive inheritance pattern and the neonatal to early childhood-onset of severe, slowly progressive, distal muscle weakness and atrophy (in particular of the peroneal group)

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ziekte van Charcot-Marie-Tooth type 4, X-gebonden

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A very rare chromosomal anomaly in which both copies of chromosome 20 are inherited from the mother. The main feature described is prenatal and postnatal growth retardation. Microcephaly, minor dysmorphic features and psychomotor developmental delay

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maternale uniparentale disomie van chromosoom 20

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https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]

Gouty arthropathy due to enzyme defects and other inherited disorders

https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]

jichtartropathie door elders geclassificeerde enzymdefecten en overige erfelijke aandoeningen

https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]

https://terminologie.nictiz.nl (...) [HTML] [2018-01-01]

Other inherited spinal muscular atrophy

https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]

overige erfelijke-vormen van spinale spieratrofie

https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]

https://terminologie.nictiz.nl (...) [HTML] [2018-01-01]

Anderen hebben gezocht naar : other inherited spinal muscular atrophy abnormality of the cytoplasm anomaly of the cytoplasm birth right council practices cytoplasmic abnormality cytoplasmic heredity cytoplasmic inheritance extra-nuclear inheritance heritage council practices inheritance council inheritance council practices inheritance law law of inheritance law of succession law on succession plasmatic heredity recessively inherited Cytoplasmic inheritance

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'Cytoplasmic inheritance' ->

Date index: 2022-10-10