parents, but her brother Alonzo has Galactosemia. Brice has asimilar family history. He and his parents are healthy, but his sister Brianna hasgalactose, a component of the lactose found in mammalian milk. Galactosemia can begalactosemia. Amanda and Brice are planning on marrying and starting a family andpartially managed by eliminating dietary intake of lactose and galactose. Amanda isGalactosemia is an autosomal recessive disorder caused by the inability to metabolizeseek genetic counseling. Based on the information provided, complete the following:healthy, as are herA piaw a pedigree that includes Amanda, Brice, their siblings, and parents. Identilythe genotypes of each person using G and a to represent the dominant andrecessive alleles.B What is the probability that Amanda is a carrier of the allele for galactosemia? Samequestion for Brice? Explain.nonbard bito teoverovoda

A pedigree chart helps to understand the presence and absence of the diseased trait in a family. It…

Aawa pedigree that includes Amanda, Brice, their siblings, and parents. ldentify the genotypes of each person using G and a to represent the dominant and recessive alleles. R What is the probability that Amanda is a carrier of the allele for galactosemia? Same question for Brice? Explain.

Aawa pedigree that includes Amanda, Brice, their siblings, and parents. ldentify the genotypes of each person using G and a to represent the dominant and recessive alleles. R What is the probability that Amanda is a carrier of the allele for galactosemia? Same question for Brice? Explain.

Human Anatomy & Physiology (11th Edition)

11th Edition

ISBN:9780134580999

Author:Elaine N. Marieb, Katja N. Hoehn

Publisher:Elaine N. Marieb, Katja N. Hoehn

Chapter1: The Human Body: An Orientation

Section: Chapter Questions

Problem 1RQ: The correct sequence of levels forming the structural hierarchy is A. (a) organ, organ system,...

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onpin=FIGIH te. G Gmail O YouTube Maps In humans, having dimples is dominant over not having dimples. In the Punnett square below, show a cross between a parent who is homozygous for dimples (DD) with a parent who is heterozygous for dimples (Dd). Then complete the table of genotypes and phenotypes for this cross. Genotypes Phenotypes Tt A Open notes navigator
Which of the following statements is true about the molecular basis of Mendel's second law? OThe random attachment of the sister chromatids and the split of them into different daughter cells during the second round of cell division in Meiosis ensure Mendel's second law of independent assortment of alleles. OThe random attachment of the sister chromatids and the split of them into different daughter cells during the first round of cell division in Meiosis ensure Mendel's 2nd law. O The molecular basis of independent assortment of alleles is the segregation of sister chromatids during the second round of cell division in Meiosis. O The molecular basis of independent assortment of alleles is the segregation of homologous chromosomes during the second round of cell division in Meiosis. O The molecular basis of independent assortment of alleles is the segregation of homologous chromosomes during the first round of cell division in Meiosis.
For the following diseases with their potential pedigree, mode of inheritance and the responsible gene: (Pedigrees A, B, and C) -> Do Pedigree A Pedigree B, Autosomal dominant, Huntingtin gene Pedigree B, Autosomal dominant, CFTR gene Pedigree B, Autosomal dominant, HexA gene Pedigree B, Autosomal dominant, FGFR3 gene Pedigree A, Autosomal recessive, CFTR gene Pedigree A, Autosomal recessive, Beta-globin gene Pedigree A, Autosomal dominant, FGFR3 gene Pedigree B, X-linked dominant. Factor VIII gene Pedigree A, Autosomal dominant, Beta-globin gene Pedigree A. Autosomal recessive, Huntingtin gene Pedigree C, X-linked recessive, Factor VIII gene Pedigree A, Autosomal recessive, HexA gene
Can you please not type the answer can you write it on a paper
Assume Mendelian inheritance laws apply, and a trait is either completely dominant or recessive. Еye color: Br – dominant brown bl – recessive blue Hair color Br" -- dominant brown bl" – recessive blonde A male with brown eyes and brown hair (genotype Br"Br"Br"bl") is planning on having a child with a female who has blue eyes and brown hair (genotype bl"bl*Br"bl"). A) Fill in all blanks (8 total to complete the two-trait Punnett Square 1). 2) Possible allelic combinations in male gametes 5) 6) 7) 8).
In this case a family history revealed a genetic basis for the disorder. The pedigree is shown in Fig. 1 Below. Key Ø Female: affected Female: unaffected || IV V 5600 orize 077808 15 10 9 10 CHO વ Male: affected Male: unaffected Deceased Disease status not given Dizygotic twins Monozygotic twins Fig. 1 Disease pedigree. Five generations I, II, III, IV, V are shown. Females are represented by circles, males by squares, dizygotic (non-identical) twins by diagonal lines originating from the same point, Monozygotic (identical) twins by diagonal lines originating from the same point and joined symbols and deceased by a diagonal line through the symbol. Filled symbols indicate that the individual displays the disease phenotype. Unfilled symbols indicate that the individual does not display the disease phenotype. Carriers of the disease are not indicated. Information on disease status is not known for generation I and is omitted for the individuals represented by a symbol with an asterisk.…
The Answer is "A" but can you tell me why the answer isn't also "C"
Dihybrid crosses and must show the Punnet square