Don’t forget your X and Y’s!

ё ё ё ё ё ё €€€€ Anticipation Guide Name: Chapter 9 Ц Frontiers in Biotechnology (page 264) I CAN : Instructions: For each of the following statements, read the textbook on the pages indicated to find the correct (T/F) answer.

They had 4 offspring. .? K» h. _______ A. How does this apply to our unit? (page 279) EVIDENCE: ________________________________________________________ & ' * O P Q V W X Y Z [ h j П ∞ х ч ю I Р С Т Ф Х Ц Ч Щ Ю чнчечеаЎћЅґЂґІ†ЬФПФЕwФrФrФЬnd_XnЬ hД … hЪЄ hД … >*hД … hД … 5Б>* hД … hД … 5БhД … hЪЄ 5БCJ \БaJ hД … hЪЄ 5Б\Б h (page 266) EVIDENCE: ________________________________________________________ T____F____3. (page 276) EVIDENCE: _____ T____F____8. æ

_____ homozygous dominant : _____ heterozygous : _____ homozygous recessive A.

Genetics and Biotechnology Unit Anticipation Guide Directions: Read each statement and decide if you agree, disagree, or are neutral about the statement. (page 276 EVIDENCE: ________________________________________________________ T____F____12. Dominant Recessive Sex-Linked Recessive Gregor Mendel figured out most of what we have talked about in genetics.

He figured out how traits are passed to offspring. Circle one: Homozygous Recessive, Homozygous Dominant, or Heterozygous. q B. 9 terms. ), -trinucleotide repeat in non-coding region, Number of repeats associated with symptomatic form of MD, -trinucleotide (GAA) repeat in non-coding region (intron of the frataxin gene), -trinucleotide repeat in a protein coding region of an autosomal gene, Normal alleles: 10-26 or fewer CAG repeats, As the BRCA1 and BRCA2 mutations are passed on in families, the telomeres of BRCA1 or 2 carriers are SHORTER than in the general population, and correlate with an increased risk of getting breast cancer at an earlier age (6.8-12.3 years earlier than their mothers) in such carriers. What is the MOST LIKELY genotype of the parents?

What is genetic anticipation. Quizlet flashcards, activities and games help you improve your grades. Draw a Punnett square of the cross RR x Rr. €€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€€м•Ѕ '` рњ bjbjLULU ." What is the probability that any female offspring will be carriers? _________ D. If you are a colorblind boy, who gave you the allele for colorblindness? Recombinant DNA is DNA from only one source. How does a trait not evident in the parents, show up in the offspring? B. A.

He figured out how traits are passed to offspring. T X F__ 1. There are many different sex determining mechanisms.

Before reading the assigned material, mark whether you agree or disagree with the statements below. D Genetics Study Guide Exam 2.

Once the correct is found, confirm your answer by writing the sentence in which you find the correct answer. B.

4 5 X øğøğøèğøğøğİÕÍÁÕͲÍÕğ Õ”‰€İÕuÍğÍğÍmğmğm hè'3 OJ QJ h[ h ¸ OJ QJ h[ 6�OJ QJ h[ h"b OJ QJ h[ h[ 6�OJ QJ "j h"b OJ QJ UmH nH u he;¶ he;¶ CJ OJ QJ aJ he;¶ he;¶ 6�OJ QJ he;¶ OJ QJ h[ OJ QJ h[ h[ OJ QJ hV OJ QJ h ¸ OJ QJ h"b OJ QJ ' Q R S Õ Ö × [ ´ µ õ E Cross a colorblind male with a normal female. The dominant allele is the allele expressed, while the recessive allele is masked by the dominant. 4 5 e ¥ ¦ ÷ î î ÷ î î æ á á ÷ Ø Ø Ğ î î Ğ î Ç º ± &. P Q S x œ Õ × Ü % P Z [ � “ ³ ´ µ ¶ ê ô õ Draw a Punnett square for a cross of RR x Rr. Colorblindness effects 7% of the CHS male population and .5% of the females. B. Circle 2: The offspring will have a: similar / different phenotype to the parents Similar / different genotype to the parents A. A.

Please follow instructions. How are females carrying this mutation affected? B. What’s the genotype for the brown-eyed person? R is Dominant for Red, r is yellow. (page 269) EVIDENCE: ________________________________________________________ T____F____11. (page 265) EVIDENCE: ________________________________________________________ T___F____9. ANTICIPATION GUIDE—INTRODUCTION TO GENETICS DECIDE IF THE FOLLOWING STATEMENTS ARE TRUE OR FALSE: 1. Biology Karyotype . Draw a punnett square for sex-linked trait. Î s Ó# ¸ ¹P 6 ÙT >U 0 nU ïP * Ä[ ‹$ ” Ä[ l T Ä[ _ T À % # # # U U % # # # nU # # # # ÿÿÿÿ ÿÿÿÿ ÿÿÿÿ ÿÿÿÿ ÿÿÿÿ ÿÿÿÿ ÿÿÿÿ ÿÿÿÿ ÿÿÿÿ ÿÿÿÿ ÿÿÿÿ ÿÿÿÿ ÿÿÿÿ ÿÿÿÿ ÿÿÿÿ ÿÿÿÿ ÿÿÿÿ Ä[ # # # # # # # # # E : What combination of alleles would results in an organism with a RECESSIVE trait? An sperm has 12 chromosomes and fertilizes an egg. Inherited genetic disorder with early onset and increased severity with each generation Caused by meiotic slippage increasing no.

How many chromosomes are in the zygote?

RR would be considered heterozygous. (page 276) EVIDENCE: ________________________________________________________ T____F____8. This post also includes the lesson plan that accompanies the handout. F How does this apply to our unit? Describe how colorblindness is passed on. Create. How does a trait not evident in the parents, show up in the offspring? Genetic Anticipation study guide by ktschauer1024 includes 14 questions covering vocabulary, terms and more. Half their kids had blue and half had brown eyes. Brave New World Anticipation Guide PDF: Brave New World Anticipation Guide PDF. Circle one .

-Maybe they are affected (soft signs of cognitive delay, poor school performance), fragile X-associated tremor/axaxia syndrome, Fragile X-associated Tremor/Ataxia Syndrome: a newly defined progressive neurologic disorder with worsening tremor and ataxia (balance disorder) affecting those older individuals carrying premutation expansions of the CGG repeat. 3. Huntington's disease (HD) - CAG- Poly Q, She suggested that a "premutation" doesn't cause severe symptoms, but as the gene was passed from generation to generation, the likelihood that this premutation would convert to a "full" mutation resulting in the classical signs of Fragile X syndrome, increased especially when passed through a female.