Do you think that karyotyping can be used to screen an embryo for genetic disorders such as sickle-cell disease that is due to a point mutation in the allele (gene) that codes for the hemoglobin protein? Explain why or why not? (hint: does a karyotype display the DNA base pair sequence of an individual?)

Talking listening and reacting non verbally are all part of communicating

An example of a trait that would be considered acquired and inherited is a. a cleft chin b. muscle tone c. scar tissue d. freckled skin

This patient undergoes a gallbladder sonogram due to epigastric pain. the report indicates that the visualized portions of the liver are normal. no free fluid noted within morisons pouch. the gallbladder is identified and is empty no evidence of wall thickening or surrounding fluid is seen there is no ductal dilation. the common hepatic duct and common bile duct measure 0.4 and 0.8 cm respectively. the common bile ductmeasurement is at the upper limits of normal what cpt code in icd-10 cm code was used