Roberts Syndrome is an extremely rare genetic disorder that is characterized by mild to severe prenatal retardation or disruption of cell division, leading to malformation of the bones in the skull, face, arms, and legs. Shown below is a pedigree for a family with Robert’s Syndrome. Based on this pedigree Roberts Syndrome is inherited as a(n) ___________ trait?





A. autosomal dominant

B. autosomal recessive

C. sex-linked dominant

D. sex-linked recessive

E. random


B. autosomal recessive

Biology & Microbiology

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