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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
Other inherited spinal muscular atrophy
Plasmatic heredity
Recessively inherited

Traduction de «cytoplasmic inheritance » (Anglais → Néerlandais) :

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

cytoplasmatische overerving | extra nucleaire overerving


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

anomalie van het cytoplasma


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

hereditary mixed polyposis syndrome


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

sensorische neuropathie | dominant erfelijk | sensorische neuropathie | recessief erfelijk | syndroom van Nelaton | ziekte van Morvan


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

erfrecht


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

praktijken van de erfgoedraad


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)

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


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

maternale uniparentale disomie van chromosoom 20


Gouty arthropathy due to enzyme defects and other inherited disorders

jichtartropathie door elders geclassificeerde enzymdefecten en overige erfelijke aandoeningen


Other inherited spinal muscular atrophy

overige erfelijke-vormen van spinale spieratrofie




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Date index: 2022-11-26
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