Notes in Week 2

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Subdecks

Name
a. DNA Sequence Variation
b. Human Genome
c. Population Genetics
d. Cytogenetics
e. Principles of Medical Genetics
f. Evidence of Genetic Factors and Multifactorial Inheritance
g. Biochemical Basis of Hereditary Disease
h. EBM
i. Genetic Counseling
j. Gene Therapy
k. Cytoskeleton

Status	Last Update	Fields
Published	07/28/2024	The symptoms of Turner syndrome are {{c1::gonadal dysgenesis}} (disappearance of eggs), {{c2:: Sexual immaturity}} (amenorrhea (absence of menstruatio…
Published	07/28/2024	The symptoms of Klinefelter syndrome are {{c1::post-pubertal testicular failure (small testes, hyalinized tubules)}}, {{c2::infertility (variable hypo…
Published	07/28/2024	Kilnefelter syndrome is present in {{c1::1/500 to 1/1000 males}}
Published	07/28/2024	Fragile X syndrome is present in {{c1::1/3500 males, 1/3300 females}}
Published	07/28/2024	Frequency of Turner syndrome is {{c1::1/5000}} females only
Published	07/28/2024	Uniparental disomy is caused by {{c1::non disjunction events during meiosis}} and amplified by {{c1::trisomy or monosomy rescue}}
Published	07/28/2024	Acrocentric chromosomes are {{c1::13, 14, 15, 21, and 22}}
Published	07/28/2024	CRISPR stands for
Published	07/28/2024	What is CAS9
Published	07/28/2024	H-W implications include predict {{c1::future (allele frequences will remain constant)}}, quick test of {{c2::population for H-W conditions}}, statist…
Status	Last Update	Fields