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Knudson - Memorial University
Knudson - Memorial University

... drawn to pediatrics. I was disappointed in the first two preclinical years because of the excessive memorization required, in great contrast to Caltech’s theme of problem solving. To my pleasant surprise, the clinical years brought me back to problem solving. Despite the fact that I was at a great m ...
Population genetics analysis of Podocnemis
Population genetics analysis of Podocnemis

... the chelonians, which are organisms that show longevity (Finch, 1990; Lutz et al., 2003). Population genetic data are one of the most important baseline components of any conservation and management plan (Frankham et al., 2002). Chelonian management, that is their conservation and breeding in captiv ...


... represents a good model for determining the relationship between genes and behaviour. Development: There are many grey areas in the area of reading and writing in the fragile X population. Very few basic and applied research studies are available and they mostly assume behavioural patterns derived f ...
Document
Document

... chemical) it became evident that the only effective combinations involved treating germinating seeds with water solutions of colchicine 0.005% x 12h and 0.05% x 2 4h (1). The obtained autotetraploids of pea (4x=28) were characterized b y changes in whole plant anatomy, morphology, and development in ...
dicer1 - Pleuropulmonary Blastoma Research
dicer1 - Pleuropulmonary Blastoma Research

... • A significant sequence abnormality IS detected, and is predicted to be associated with a genetic disease. • A sequence abnormality IS detected, but its significance is UNKNOWN. Additional testing of the patient and/or other family members may be recommended to help determine the significance of th ...
Genetics and Genomics in Medicine Chapter 5 Questions Multiple
Genetics and Genomics in Medicine Chapter 5 Questions Multiple

... With respect to X-chromosome inactivation in females, which, if any, of the following statements is incorrect? a) X-inactivation first occurs in the preimplantation female mammalian embryo. b) One of the two X chromosomes in each diploid cell of a normal woman is randomly selected to undergo X-inact ...
Genetic Disorder Powerpoint Project
Genetic Disorder Powerpoint Project

... a 12 slide presentation using multimedia presentation software such as PowerPoint on a specific genetic disorder. Background knowledge: You have already completed your basic study about the ideas of genetics and mutations. Now with the information that you have you are being asked to research a spec ...
Genetics Concept Check Answers Concept Check 10.1 Particulate
Genetics Concept Check Answers Concept Check 10.1 Particulate

Biology~Chapter 12
Biology~Chapter 12

... • Fragile-X syndrome- part of X chromosome has errors- most common cause of mental retardation in males • Red-green color blindness- males cannot see these 2 colors. ...
Examples
Examples

... they realize they have it – Forgetfulness, irritability, muscle spasms and mental illness, then death – Genetic testing now beginning to be used to determine if either parent has disease ...
Grade12GeneticEngineering
Grade12GeneticEngineering

... — Ian Wilmut The Second Creation: Dolly and the Age of Biological Control ...
Mendelian Genetics
Mendelian Genetics

...  Type O – no sugar marker - OO  Type A ...
11–3 Exploring Mendelian Genetics
11–3 Exploring Mendelian Genetics

... Many genes exist in several different forms, and are therefore said to have multiple alleles. An individual can’t have more than two alleles in their cells. However, more than two possible alleles for each trait can exist in a population. A rabbit's coat color is determined by a single gene that has ...
RGC Collaborator Factsheet
RGC Collaborator Factsheet

... as part of this project; Mayo Clinic and University of Kiel have contributed DNA samples from nearly 2,500 consented PSC patients and many more including primary biliary cirrhosis, healthy volunteers and inflammatory bowel disease (which is strongly associated with and has a high co-occurrence rate i ...
SCI24TutDec2nd - Rocky View Schools
SCI24TutDec2nd - Rocky View Schools

... while males have one x or one y chromosome. When an egg is fertilized with an Xcontaining sperm, the offspring is XX (girl), when an egg is fertilized by a y-containing sperm, the offspring is XY, a male. In lesson 6, you will be learning about Gregor Mendel’s work with pea plants and how he learned ...
Chapter 14 * The Human Genome
Chapter 14 * The Human Genome

... In Turner’s syndrome, a female is only born with one X chromosome  as a result her sex organs do not develop at puberty and she is sterile In Klinefelter’s syndrome, males end up with an extra X chromosome There has not been a case where a baby was born without an X chromosome, showing that its gen ...
The Legal Implications of Behavior Genetics Research
The Legal Implications of Behavior Genetics Research

... had on the verdict.13 Additionally, in a French case, a man who strangled a prostitute was given a reduced sentence based on his XYY syndrome.14 These results bring to light the court’s important role in determining what evidence is scientific enough to use. The French case in particular is disturbi ...
11.1 Genetic Variation Within Population
11.1 Genetic Variation Within Population

... that some individuals will survive. • Genetic variation leads to phenotypic variation. • Phenotypic variation is necessary for natural selection. • Genetic variation is stored in a population’s gene pool. – made up of all alleles in a population – allele combinations form when organisms have offspri ...
Genetics in Epidemiology - University of Pittsburgh
Genetics in Epidemiology - University of Pittsburgh

... • Is there evidence of familial aggregation of the disorder (phenotype)? – Is a positive family history an independent risk factor for the disorder? • For many chronic disorders, a positive family history is associated with odds ratios between 2-6 ...
Genetic Disorder Powerpoint Project
Genetic Disorder Powerpoint Project

... Slide 2) What is the name of the disorder, who gets it, and how common is it? Slide 3) What are the signs and symptoms of the disease. What systems of the body does it affect and how does it affect them? What parts of the cell does it affect and how? Slide 4) How is the disease diagnosed and what is ...
Ch. 14 The Human Genome-Sec. 1 Human Heredity
Ch. 14 The Human Genome-Sec. 1 Human Heredity

... are carriers for sickle cell disease. Children who receive a recessive gene from each parent can become blind. Arms and legs can become paralyzed or even die. Strokes and heart attacks are common. Treatments are available to decrease the complications of this disease but there is no cure. Many Afric ...
Slide 1
Slide 1

... – Copy Number Variants (CNVs) • Indels > 1Kb in size ...
Honors Biology - WordPress.com
Honors Biology - WordPress.com

... 3. In sexual reproduction, each parent contributes only one allele to the offspring. 4. This is why meiosis takes diploid cells and makes them haploid. The process of meiosis separates the homologous pairs, separating the alleles from each other. Each gamete (sperm and egg) when fused will result wi ...
Metabolic disease resources - Zurich Open Repository and Archive
Metabolic disease resources - Zurich Open Repository and Archive

... Definition Metabolic disease resources include several databases that provide information on the causes, clinical manifestations, as well as diagnostic and genetic indicators of metabolic diseases. These resources are often extensively cross-linked to databases containing gene, protein and metabolit ...
Study Guide Genetics Final 2014
Study Guide Genetics Final 2014

... 2. How is an autosome different from a sex chromosome? 3. How is an X different from a y chromosome? 4. Use a Punnet square to show how gender is passed from parent to offspring. Which parent’s chromosome determines the sex of a child? Why? 5. Compare and contrast dominant and recessive alleles. Wha ...
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Medical genetics

Medical genetics is the specialty of medicine that involves the diagnosis and management of hereditary disorders. Medical genetics differs from human genetics in that human genetics is a field of scientific research that may or may not apply to medicine, but medical genetics refers to the application of genetics to medical care. For example, research on the causes and inheritance of genetic disorders would be considered within both human genetics and medical genetics, while the diagnosis, management, and counseling of individuals with genetic disorders would be considered part of medical genetics.In contrast, the study of typically non-medical phenotypes such as the genetics of eye color would be considered part of human genetics, but not necessarily relevant to medical genetics (except in situations such as albinism). Genetic medicine is a newer term for medical genetics and incorporates areas such as gene therapy, personalized medicine, and the rapidly emerging new medical specialty, predictive medicine.
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