
Genetic Disorders Mendelian Disorders
... Congenital malformations of the heart are present in over half of these persons, and there is a 15-fold increase in risk for developing leukemia. Characteristic face and physique. ...
... Congenital malformations of the heart are present in over half of these persons, and there is a 15-fold increase in risk for developing leukemia. Characteristic face and physique. ...
Midterm Study Guide 1
... hypothalamus, cerebral cortex, cerebellum, glial cells, myelin sheath 11-Know the three messengers in the body: neurotransmitters, endorphins, and hormones. 12- Know the function of the endocrine system. 13-Know the function of the lobes of the brain ...
... hypothalamus, cerebral cortex, cerebellum, glial cells, myelin sheath 11-Know the three messengers in the body: neurotransmitters, endorphins, and hormones. 12- Know the function of the endocrine system. 13-Know the function of the lobes of the brain ...
How to be a clinical geneticist
... • Half of our chromosomes and genes come from a maternal egg – half from the sperm • All these 46 chromosomes contain all the information needed to create a whole baby • As the cells divide, the DNA is copied over and over into each new cell ...
... • Half of our chromosomes and genes come from a maternal egg – half from the sperm • All these 46 chromosomes contain all the information needed to create a whole baby • As the cells divide, the DNA is copied over and over into each new cell ...
Ch 7 Mendel Powerpoint
... How can you tell if a chromosome is a autosome or a sex chromosome? If the same # of male & female have the phenotype then the gene is most likely ...
... How can you tell if a chromosome is a autosome or a sex chromosome? If the same # of male & female have the phenotype then the gene is most likely ...
Study Guide for Exam # 3 - HCC Learning Web
... 1. Understand the basic terms discussed in class. You do not need to provide the textbook definition word by word, but be able to understand their meaning: gene, locus, haploid, diploid, gametes, etc. 2. Asexual versus sexual reproduction: Understand them. 3. Sets of chromosomes in human cells: How ...
... 1. Understand the basic terms discussed in class. You do not need to provide the textbook definition word by word, but be able to understand their meaning: gene, locus, haploid, diploid, gametes, etc. 2. Asexual versus sexual reproduction: Understand them. 3. Sets of chromosomes in human cells: How ...
Name: Sex-Linked Inheritance The study of inheritance of genes
... The study of inheritance of genes located on sex chromosomes was pioneered by T. H. Morgan and his students at the beginning of the 20th century. Although Morgan studied fruit flies (Drosophila), the same genetic principles apply to humans. A. Some genes on sex chromosomes play a role in sex determi ...
... The study of inheritance of genes located on sex chromosomes was pioneered by T. H. Morgan and his students at the beginning of the 20th century. Although Morgan studied fruit flies (Drosophila), the same genetic principles apply to humans. A. Some genes on sex chromosomes play a role in sex determi ...
2. Notes
... • In sympatric speciation, a reproductive barrier isolates a subset of a population without geographic separation from the parent species • Sympatric speciation can result from polyploidy, natural selection, or sexual selection ...
... • In sympatric speciation, a reproductive barrier isolates a subset of a population without geographic separation from the parent species • Sympatric speciation can result from polyploidy, natural selection, or sexual selection ...
Cells, Development, Chromosomes
... polyploid: having more than 2 sets of chromosomes. aneuploid: having an extra copy or a missing copy of a single chromosome. (equal numbers of all chromosomes is euploid). mixoploid: having cell lines with different chromosomal constitutions. – mosaics: derived from a single zygote. After a few cell ...
... polyploid: having more than 2 sets of chromosomes. aneuploid: having an extra copy or a missing copy of a single chromosome. (equal numbers of all chromosomes is euploid). mixoploid: having cell lines with different chromosomal constitutions. – mosaics: derived from a single zygote. After a few cell ...
Unit 2 Review 1. Define the following terms: a. Meiosis b
... 3. What is the total number of chromosomes that the average person has in a sex cell? 4. How many pairs of chromosomes does the average person have in a somatic cell? 5. What is a human’s diploid number (2n)? 6. What is a human’s haploid number (n)? 7. Is a human somatic cell diploid or haploid? 8. ...
... 3. What is the total number of chromosomes that the average person has in a sex cell? 4. How many pairs of chromosomes does the average person have in a somatic cell? 5. What is a human’s diploid number (2n)? 6. What is a human’s haploid number (n)? 7. Is a human somatic cell diploid or haploid? 8. ...
lab9 - Java JAVAC
... their possible genotypes for a variety of traits and then predict the probability of their children having those traits. Use Punnett squares to answer questions in your packet. ...
... their possible genotypes for a variety of traits and then predict the probability of their children having those traits. Use Punnett squares to answer questions in your packet. ...
(DOCX, Unknown)
... C) Each cell has eight homologous pairs. D) During the S phase of the cell cycle there will be 32 separate chromosomes. E) A gamete from this species has four chromosomes. 47) Which of these statements is false? A) In humans, each of the 22 maternal autosomes has a homologous paternal chromosome. B) ...
... C) Each cell has eight homologous pairs. D) During the S phase of the cell cycle there will be 32 separate chromosomes. E) A gamete from this species has four chromosomes. 47) Which of these statements is false? A) In humans, each of the 22 maternal autosomes has a homologous paternal chromosome. B) ...
Changes in chromosome number
... and this inactivation persists throughout all subsequent mitotic divisions – Barr bodies: an ...
... and this inactivation persists throughout all subsequent mitotic divisions – Barr bodies: an ...
cladogram analysis
... 3. (__________________________)- flea and a cat. 4. (__________________________)- buffalo and an insect eating bird 5. (__________________________)- organisms living together 6. A wasp injecting eggs into another organism. As the eggs develop into larvae, they use the host for nutrients. The host di ...
... 3. (__________________________)- flea and a cat. 4. (__________________________)- buffalo and an insect eating bird 5. (__________________________)- organisms living together 6. A wasp injecting eggs into another organism. As the eggs develop into larvae, they use the host for nutrients. The host di ...
Introduction Thomas Hunt Morgan
... • In human and other mammals, there are two varieties of sex chromosomes, X and Y. – An individual who inherits two X chromosomes usually develops as a female. – An individual who inherits an X and a Y chromosome usually develops as a male. ...
... • In human and other mammals, there are two varieties of sex chromosomes, X and Y. – An individual who inherits two X chromosomes usually develops as a female. – An individual who inherits an X and a Y chromosome usually develops as a male. ...
Heredity
... In the early 1900s, Walter Sutton, an American geneticist, looked at chromosomes in grasshoppers His hypothesis was that chromosomes are the key to understanding how traits are passed from parents to offspring Sutton discovered that sex cells in grasshoppers (sperm and egg cells) only had half the n ...
... In the early 1900s, Walter Sutton, an American geneticist, looked at chromosomes in grasshoppers His hypothesis was that chromosomes are the key to understanding how traits are passed from parents to offspring Sutton discovered that sex cells in grasshoppers (sperm and egg cells) only had half the n ...
File
... So, a few offspring would be TtBB and TTBb, which would be recombinants! (different genotype than either parent). ...
... So, a few offspring would be TtBB and TTBb, which would be recombinants! (different genotype than either parent). ...
4 BLY 122 Lecture Notes (O`Brien) 2006 II. Protists (Chapter 28) A
... 2. Organelles in single-celled protists perform same functions that are accomplished by organ systems multi-celled eukaryotes Picture Slide Fig 28.12 Protists have specialized intracellular structures. 3. The evolution of multicellularity a. Protistans may be unicellular, colonial, or multicellular. ...
... 2. Organelles in single-celled protists perform same functions that are accomplished by organ systems multi-celled eukaryotes Picture Slide Fig 28.12 Protists have specialized intracellular structures. 3. The evolution of multicellularity a. Protistans may be unicellular, colonial, or multicellular. ...
Chapter Three
... Produces incremental random changes (with very low probability) in the offsprings by changing allele values of some genes Mutation perturbs a chromosome in order to introduce new characteristics not present in any element of the population Example: Swap two alleles, toggle one or two (in case of bin ...
... Produces incremental random changes (with very low probability) in the offsprings by changing allele values of some genes Mutation perturbs a chromosome in order to introduce new characteristics not present in any element of the population Example: Swap two alleles, toggle one or two (in case of bin ...
How did I get this? Prenatal and neonatal screening Ultrasound
... Such congenital disorders can be caused by external factors such as intake of alcohol, medication or drugs, infectious diseases during pregnancy, or problems that develop during labour. Such factors cause disorders in which the baby’s genetic information remains unchanged and which are therefore not ...
... Such congenital disorders can be caused by external factors such as intake of alcohol, medication or drugs, infectious diseases during pregnancy, or problems that develop during labour. Such factors cause disorders in which the baby’s genetic information remains unchanged and which are therefore not ...
Tic Tac Toe 1 - Northwest ISD Moodle
... 1. What are alleles? ANSWER: Alternate forms (variations) of a gene, Example: Brown eyes, Green eyes, Blue eyes 2. Two rabbits are crossed. Tan fur is dominant over white fur. 50% of the are tan and 50% are white. What are the genotypes of the parents? ANSWER: Tt and tt 3. If you cross someone with ...
... 1. What are alleles? ANSWER: Alternate forms (variations) of a gene, Example: Brown eyes, Green eyes, Blue eyes 2. Two rabbits are crossed. Tan fur is dominant over white fur. 50% of the are tan and 50% are white. What are the genotypes of the parents? ANSWER: Tt and tt 3. If you cross someone with ...
Basic genetics: Directed-study File
... you. Therefore, you should read the chapters on genetics in Atkinson & McHanwell or Tortora • Some of the slides have notes attached, so you might like to print off as ‘notes pages’ to assist you ...
... you. Therefore, you should read the chapters on genetics in Atkinson & McHanwell or Tortora • Some of the slides have notes attached, so you might like to print off as ‘notes pages’ to assist you ...
Document
... 1) Sex Chromosomes: determine a person’s gender. *Female = XX *Male = XY 2) Autosomes: All 44 other chromosomes (not sex chromosomes). 3) During reproduction, there is a 50/50 chance of getting a boy or girl. a) A gamete carries 22 autosomes and one sex chromosome. * Egg cells carry only X chromosom ...
... 1) Sex Chromosomes: determine a person’s gender. *Female = XX *Male = XY 2) Autosomes: All 44 other chromosomes (not sex chromosomes). 3) During reproduction, there is a 50/50 chance of getting a boy or girl. a) A gamete carries 22 autosomes and one sex chromosome. * Egg cells carry only X chromosom ...
Honors BIOLOGY
... males get only one X chromosome (always from mom), if that gene is faulty then there is no allele on the Y to override it and the male is affected. Because females get two X’s, they have two chances to be normal. Sex-linked genotypes always use the XX or XY sex genotypes “carrying” the linked trait ...
... males get only one X chromosome (always from mom), if that gene is faulty then there is no allele on the Y to override it and the male is affected. Because females get two X’s, they have two chances to be normal. Sex-linked genotypes always use the XX or XY sex genotypes “carrying” the linked trait ...
Chromosome_Mutations_Tutorial_2015
... Chromosome Mutations Reading Tutorial INTRODUCTION The sperm and egg cells (gametes) required for sexual reproduction are produced by meiotic cell division. Gametes are haploid cells. In humans, each gamete contains 23 chromosomes (22 are autosomes and 1 sex chromosome; either X or Y). In males, the ...
... Chromosome Mutations Reading Tutorial INTRODUCTION The sperm and egg cells (gametes) required for sexual reproduction are produced by meiotic cell division. Gametes are haploid cells. In humans, each gamete contains 23 chromosomes (22 are autosomes and 1 sex chromosome; either X or Y). In males, the ...
Ploidy
Ploidy is the number of sets of chromosomes in a cell. Usually a gamete (sperm or egg, which fuse into a single cell during the fertilization phase of sexual reproduction) carries a full set of chromosomes that includes a single copy of each chromosome, as aneuploidy generally leads to severe genetic disease in the offspring. The gametic or haploid number (n) is the number of chromosomes in a gamete. Two gametes form a diploid zygote with twice this number (2n, the zygotic or diploid number) i.e. two copies of autosomal chromosomes. For humans, a diploid species, n = 23. A typical human somatic cell contains 46 chromosomes: 2 complete haploid sets, which make up 23 homologous chromosome pairs.Because chromosome number is generally reduced only by the specialized process of meiosis, the somatic cells of the body inherit and maintain the chromosome number of the zygote. However, in many situations somatic cells double their copy number by means of endoreduplication as an aspect of cellular differentiation. For example, the hearts of two-year-old children contain 85% diploid and 15% tetraploid nuclei, but by 12 years of age the proportions become approximately equal, and adults examined contained 27% diploid, 71% tetraploid and 2% octaploid nuclei.Cells are described according to the number of sets present (the ploidy level): monoploid (1 set), diploid (2 sets), triploid (3 sets), tetraploid (4 sets), pentaploid (5 sets), hexaploid (6 sets), heptaploid or septaploid (7 sets), etc. The generic term polyploid is frequently used to describe cells with three or more sets of chromosomes (triploid or higher ploidy).