The Effects of Genetics Diseases due to Chromosomal Abnormalities and DNA mutations Nondisjunction Nondisjunction occurs when homologous chromosomes fail to separate ...
Human Genetic Disorders Harmful or Beneficial? Human Genetic Disorders Mutations are key DNA change change in alleles Chromosomal errors nondisjunction Deletion ...
Inheritance Patterns & Human Genetics Ch.12 Sex-Influenced Traits Presence of sex hormones influences expression of these traits Ex: Pattern baldness Nondisjunction ...
Types of Chromosome Mutations Aneuploidy (2n +/- m) Aneuploids differ from wild-type individuals by part of a chromosome set. Nondisjunction is a common mechanism for ...
... transmitted by genes or chromosomal aberrations, that may be heritable ... NONDISJUNCTION (Chromosomal numerical ... I. MORPHOLOGIC/ STRUCTURAL ...
Defects in Chromosome Structure. translocations. deletions, duplications. Chromosome Nondisjunction. XX. X. X. nondisjunction. nondisjunction. XX. XX. N. N ...
Color blindness is a sex-linked trait in humans. In humans, the X chromosome has ... Pedigree analysis. Nondisjunction. Turner's Syndrome. Klinefelter Syndrome ...
Human Genetics. Diseases Caused by Nondisjunction. Definition. Sample Problems. Down Syndrome ... Restriction fragment length polymorphisms (RFLPs) Autosomal ...
Types of Genetic Mutations Main Types Base Substitutions Gene Rearrangements Nondisjunction Base Substitutions Also known as point mutations, result when one ...
Mitosis and Meiosis Review When does nondisjunction occur? (during what phases) Anaphase I or Anaphase II True or False? During telophase, a nuclear envelope ...
There are many steps between genotype and phenotype; genes cannot ... Nondisjunction and translocations can occur. 1. 2. Mutations: Heritable Changes in Genes ...
What happens when Meiosis Goes WRONG?? When homologous chromosomes fail to separate it is called nondisjunction Abnormal # chromosomes will make their way into ...
Alterations of chromosome number, nondisjunction, aneuploidy, monosomy, trisomy, ... When the mother is a dominant homozygote, the daughters will have the normal ...
Affect parts of a chromosome rather than whole thing. Reciprocal translocations ... In diploids: Results in either half OR no normal gametes. Nondisjunction in ...
... of trisomy involves three copies of chromosome 21 and is called Down syndrome. Down's Syndrome ... syndrome. In males, nondisjunction causes Klinefelter's ...
effects of Down Syndrome vary greatly from person to person but can include mild ... Down Syndrome. Kleinfelter's (XXY) results from nondisjunction of the sex ...
Meiosis I separation of homologous chromosomes (in 4-5 steps: prophase I, metaphase I, anaphase I, ... Nondisjunction. Karyotype. Spermatogenesis & Oogenesis ...
Caused by nondisjunction of the sex chromosomes. Characteristics of Turner's Syndrome: ... gene that causes a mutation on chromosome 4 ... gene on chromosome 7 ...
Gametes have one set of chr. This is called haploid cell ... Nondisjunction results in gamete with extra chr. If other gamete is normal zygote will have 2n 1 ...
Title: Genetics Lesson 2: Mistakes in Meiosis Author: Victor and Molly Last modified by: Victor and Molly Document presentation format: Custom Other titles
Chromosomal Mutations & their effects Karyotype A picture of the chromosomes of an individual or a species, including number, form, and size of the chromosomes.
Mistakes in Meiosis Including Mutations & Non-disjunction What is a Gene? A gene is the basic unit of heredity in a living organism Genes hold the information to ...
... Trisomy 21 (Down), Trisomy 18 (Edward), Trisomy 13 ... Jacob syndrome individual ... 2. 5% of Down syndrome result of translocation between chromosomes 21 ...
Cytogenetics Chromosomal Disorders 50% of 1st trimester miscarriages 5% of stillbirths 0.5% of liveborns Down syndrome trisomy 21 Fragile X syndrome Somatic cell ...
Genetic Mutations Mutations Mutations: changes in the DNA They may not change the individual in a way that impacts their reproductive success or They can be damaging.
Chromosomal Disorders Amniocentesis Single Chromosome Disorders Deletion Genetic material is missing 2. Duplication Genetic material is present twice 3.
Title: 14-2 Human Chromosomes Author: Kelso Last modified by: Craig Kelso Created Date: 3/25/2002 6:04:52 AM Document presentation format: On-screen Show (4:3)
Chromosome Disorders Prenatal Diagnosis Amniocentesis A small sample of the amniotic fluid surrounding the baby is removed using a syringe. The fluid contains skin ...
Human Heredity. Vocabulary. Karyotype. Sex chromosome. Autosome. pedigree. What are the types of chromosomes in a karyotype. 46 chromosomes = 23 from dad. 23 from mom ...
... Wheat and Wolverines all have 42 chromosomes Karyotypes A karyotype is a picture of an organisms chromosomes It allows us to study the difference of shape, ...
The women are sterile and their sex organs do not develop at puberty. ... The Human Genome Sex chromosome = one of two chromosomes that determine an individual s ...
Karyotypes and Sex-Linked Traits What is a karyotype? Picture of your chromosomes Arranged from largest to smallest quickly identify chromosomal changes http://www ...
CHROMOSOMAL ABNORMALITIES By Dr Samina Anjum s particular translocation is interesting because * * CAUSES OF BIRTH DEFECTS & SPONTANEOUS ABORTIONS ARE Chromosomal ...
Human Genetics Chapter 14 Human Chromosomes How many kinds of chromosomes do humans have? 23 How many chromosomes do humans have? 46 (23 from each parent) What are ...
This type of mutation can be passed to the zygote and show up in ... the resulting gametes has an extra chromosomes while the other gamete lacks a chromosome. ...
Mutations * * * * * * * * * * * * * * * * * * * What Are Mutations? Changes in the nucleotide sequence of DNA May occur in somatic cells (aren t passed to offspring ...
Chromosomal Mutations & their effects Karyotype A picture of the chromosomes of an individual or a species, including number, form, and size of the chromosomes.