User contributions
From Iusmgenetics
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- 16:39, 2 December 2011 (hist) (diff) Complex Diseases (top)
- 16:15, 2 December 2011 (hist) (diff) N Complex Diseases (Created page with '=Genetic Mapping of Complex Disease= ==Complex Disease== *Both genes and environmental factors contribute to disease risk *Genetic diseases seen most often in clinical practice …')
- 15:56, 2 December 2011 (hist) (diff) N Mapping of Mendelian Disorders (Created page with '*See PDF annotations') (top)
- 17:23, 30 November 2011 (hist) (diff) Cancer Genetics
- 16:18, 30 November 2011 (hist) (diff) Cancer Genetics
- 15:16, 30 November 2011 (hist) (diff) N Cancer Genetics (Created page with '=Cancer Genetics= ==Objectives== *Understand that cancer is a genetic disease and a multistep process. *Know the types of genes associated with cancer. *Know fundamentals about …')
- 14:12, 28 November 2011 (hist) (diff) Molecular and Biochemical Genetics (→Newborn Screening)
- 13:31, 28 November 2011 (hist) (diff) Main Page
- 13:27, 28 November 2011 (hist) (diff) Hemophilia A
- 13:24, 28 November 2011 (hist) (diff) Unusual Molecular Pathogenesis (top)
- 13:23, 28 November 2011 (hist) (diff) Charcot-Marie-Tooth Disease (top)
- 13:20, 28 November 2011 (hist) (diff) Unusual Molecular Pathogenesis
- 13:17, 28 November 2011 (hist) (diff) Polycystic Kidney Disease (top)
- 13:10, 28 November 2011 (hist) (diff) Huntington Disease (top)
- 12:59, 28 November 2011 (hist) (diff) Fragile-X Syndrome
- 12:31, 28 November 2011 (hist) (diff) Myotonic Dystrophy (top)
- 23:18, 18 October 2011 (hist) (diff) Inherited Muscular Dystrophies (top)
- 23:08, 18 October 2011 (hist) (diff) Lesch-Nyhan syndrome (top)
- 23:05, 18 October 2011 (hist) (diff) Rett Syndrome (top)
- 23:00, 18 October 2011 (hist) (diff) Alpha-1-Anti-Trypsin deficiency
- 22:56, 18 October 2011 (hist) (diff) Hemochromatosis
- 22:52, 18 October 2011 (hist) (diff) Cystic Fibrosis
- 22:16, 18 October 2011 (hist) (diff) N Charcot-Marie-Tooth Disease (Created page with '==Charcot-Marie-Tooth Disease== ===General background information=== *Charcot-Marie-Tooth disease is also known as '''"Hereditary motor and sensory neuropathy"''' (HMSN) ===Mod…')
- 22:15, 18 October 2011 (hist) (diff) Unusual Molecular Pathogenesis
- 22:13, 18 October 2011 (hist) (diff) Unusual Molecular Pathogenesis (→Unstable repeat expansion)
- 22:05, 18 October 2011 (hist) (diff) N Hemophilia A (Created page with '==Hemophilia A== ===General background information=== ===Mode of inheritance=== *'''X-linked recessive''' ===Single important gene=== *The FVIII gene makes the clotting cascad…')
- 21:49, 18 October 2011 (hist) (diff) N Neurofibromatosis (Created page with '==Neurofibromatosis== ===General background information=== *There are two types (I and II) **'''type I is the most common''' so that's what we'll describe here **Type I = von Re…') (top)
- 21:40, 18 October 2011 (hist) (diff) N Polycystic Kidney Disease (Created page with '==Disease Name== ===General background information=== ===Mode of inheritance=== *Autosomal dominant **One of the most common dominant diseases in humans. *1/300 - 1/1000 births…')
- 21:34, 18 October 2011 (hist) (diff) N Huntington Disease (Created page with '==Huntington Disease== ===General background information=== ===Mode of inheritance=== *'''Autosomal dominant''' *97% of cases are inherited *Because of anticipation, there are …')
- 21:15, 18 October 2011 (hist) (diff) N Fragile-X Syndrome (Created page with '==Fragile X Syndrome== ===General background information=== *Called "Fragile X" because in a certain subset the conditions are right for an end of the X chromosome to fall off. …')
- 20:25, 18 October 2011 (hist) (diff) N Myotonic Dystrophy (Created page with '==Myotonic Dystrophy== ===General background information=== *'''Most common inherited neuromuscular disorder of adult life''' ===Mode of inheritance=== *'''Autosomal dominant''…')
- 20:09, 18 October 2011 (hist) (diff) Unusual Molecular Pathogenesis (→Unstable repeat expansion)
- 20:01, 18 October 2011 (hist) (diff) Unusual Molecular Pathogenesis
- 19:53, 18 October 2011 (hist) (diff) N Unusual Molecular Pathogenesis (Created page with '==Unusual Molecular Pathogenesis== ===Objectives=== *Know the concepts: **Unstable repeat expansions **Two hit phenomenon **Alterened gene structure / dose from unusual crossove…')
- 19:32, 18 October 2011 (hist) (diff) Tay-Sachs Disease
- 19:22, 18 October 2011 (hist) (diff) Molecular and Biochemical Genetics
- 19:21, 18 October 2011 (hist) (diff) Maple Syrup Urine Disease (top)
- 19:16, 18 October 2011 (hist) (diff) Cystic Fibrosis
- 19:11, 18 October 2011 (hist) (diff) N Biotinidase Deficiency (Created page with '==Biotinidase Deficiency== ===General background information=== *1 / 61K *Most common in French Canadians *'''An inability to release biotin form proteins and recycle it or a pr…') (top)
- 19:00, 18 October 2011 (hist) (diff) Molecular and Biochemical Genetics
- 18:59, 18 October 2011 (hist) (diff) Maple Syrup Urine Disease
- 16:53, 18 October 2011 (hist) (diff) N Galactosemia (Created page with '==Galactosemia== ===General background information=== *Galactosemia encompasses '''3 autosomal recessive disorders''': galactose 1-p uridyltransferase (GALT), galactokinase, epi…') (top)
- 16:25, 18 October 2011 (hist) (diff) Template for diseases (top)
- 16:25, 18 October 2011 (hist) (diff) N Tay-Sachs Disease (Created page with '==Tay-Sachs Disease== ===General background information=== *Tay-Sachs disease is a lysosomal storage disease secondary to HexA deficiency and GM2 accumulation. *Tay-Sachs primar…')
- 16:24, 18 October 2011 (hist) (diff) Molecular and Biochemical Genetics
- 15:34, 18 October 2011 (hist) (diff) N Phenylketonuria (Created page with '==Phenylketonuria (PKU)== ===General background information=== ===Mode of inheritance=== *Autosomal recessive *Demonstrates allelic heterogeneity **>400 known disease causing m…')
- 15:34, 18 October 2011 (hist) (diff) Molecular and Biochemical Genetics
- 14:36, 18 October 2011 (hist) (diff) Molecular and Biochemical Genetics
- 14:26, 18 October 2011 (hist) (diff) Homocysteinuria (top)
- 14:04, 18 October 2011 (hist) (diff) N Maple Syrup Urine Disease (Created page with '==Disease Name== ===General background information=== ===Mode of inheritance=== ===Single important gene=== ===Etiology=== ===Pathogenesis=== ===Phenotypic information=== …')
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