Answer:
squamous epithelium maybe
Answer:
The correct answer is d) genomic imprinting.
Explanation:
Genomic imprinting is a biological process by which specific modifications in the germ line that produce differences in the expression of the genetic material that is biochemically marked indicating its parental origin. The Prader-Willi syndrome is one of the best known and most studied examples in relation to pathologies produced by genomic imprinting. Prader-Willi syndrome is a complex genetic disease that is fundamentally neurological. Its appearance is due to a deletion of a fragment of chromosome 15 derived from the father.
Blood type doesn't fall into the category of dominant/recessive genes exactly; rather it combines this with the properties of incomplete dominance. Ignoring the Rh factor, there are 3 alleles for blood type, I^a,I^b, and i. You will be type A if you have I^a I^a or I^a i and type B if you have I^b I^b or I^b i. You can also get type AB by having the combination I^a I^b or be type O if you have i i. If you need to use dominant/recessive, you can say the A and B allele are dominant over the O allele and codominant with one another.
Answer:
<em>The correct option is d) an ecotone</em>
Explanation:
An ecotone can be described as an area of transition between two different biomes. An estuary can be described as an ecotone where the river water meets the seawater. The freshwater biome mixes with the seawater biome in an estuary. Unique plants and animals are grown in an estuary which are adapted to live in such an environment. The water present in an estuary is termed as brackish water. Hence, the correct option is d.
Answer:
<h3>
Qu'est-ce que l'ADN ?</h3>
L'ADN (acide désoxyribonucléique) est un type d'acide nucléique qui se distingue par le stockage de l'information génétique de la grande majorité des êtres vivants. Cette molécule est formée de nucléotides et a généralement la forme d'une double hélice.
Il est nécessaire de prélever des échantillons de certains fluides corporels qui peuvent être du sang, de la salive, des ongles, des cheveux ou du sperme. À l'aide de techniques de laboratoire sophistiquées, l'ADN des échantillons est isolé, puis une cartographie est effectuée, ce qui est fait par des équipements appelés "Séquenceurs d'ADN".
Pour le prouver, normalement le rapport d'un examen ADN apporte quels gènes et chromosomes ont été étudiés et l'analyse du généticien à leur sujet. Les résultats sont présentés dans des rapports simples et clairs. Dans les examens de paternité, le résultat est toujours comparatif.
J'espère t'avoir aidé, bonnes études !
