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By virtue of heredity
Cytoplasmic heredity
Cytoplasmic inheritance
Extra-nuclear inheritance
Gene pool
Genetic resource
Genetic stock
Genetics
Genotype
Heredity
Monogene
Monogenetic
Monogenic
Monogenic disease
Monogenic disorder
Monogenic heredity
Monogenic resistance
Multifactorial cumulative heredity
Multifactorial heredity
Plasmatic heredity

Vertaling van "monogenic heredity " (Engels → Frans) :



monogenic disease | monogenic disorder

maladie monogène | maladie héréditaire monogénique


Melanocortin 4 receptor (MC4R) deficiency is the commonest form of monogenic obesity identified so far. MC4R deficiency is characterized by severe obesity, an increase in lean body mass and bone mineral density, increased linear growth in early child

obésité par déficit du récepteur de la mélanocortine 4




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

hérédité cytoplasmique | héritage cytoplasmique | héritage extra-nucléaire


genetics [ gene pool | genetic resource | genetic stock | genotype | heredity | heredity(UNBIS) ]

génétique [ hérédité | patrimoine génétique | ressource génétique ]


multifactorial cumulative heredity | multifactorial heredity

hérédité polymérique


Prohormone convertase-I deficiency is the rarest form of monogenic obesity. The disorder is characterized by severe childhood obesity, hypoadrenalism, reactive hypoglycemia, and elevated circulating levels of certain prohormones. It has been describe

obésité par déficit en prohormone convertase I








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Date index: 2021-02-22
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