The most common form of hemophilia is a defect in blood clotting factor VIII, which is caused by a mutant form of a gene on the X chromosome. Boys who inherit that mutation from their mother suffer from uncontrolled bleeding. Girls carrying one copy of this mutation have near normal blood clotting. Uncommonly, a girl is born with hemophilia even though both parents have normal phenotypes. Which of the statements might explain hemophilia in a girl born to parents with normal blood clotting phenotypes?

this protocol provides a detailed procedure for nucleoprotein extraction from cultured cells and tissues in an efficient manner.

children tend to take more after their grandparents more than their parents. it’s the dna you received that was passed down to you somewhere in your family. maybe one of your grandparents had/has straight hair and you might have gotten it from them.

one is through turgidity. this occurs before ground tissue ( collenchyma

and sclerenchyma cells) become well

developed to give structural support to the plant as it grows bigger. the xylem

tissue (composed of rigid tissue) of the young

plant render this support and also maintaining osmotic turgidity of the surrounding

plant cells.