for Specific Topics

Nov 27, 2016 by in GENERAL & FAMILY MEDICINE Comments Off on for Specific Topics

References for Specific Topics Arora N, Daley GQ. Pluripotent stem cells in research and treatment of hemoglobinopathies. Cold Spring Harb Perspect Med. 2012;2:a011841. Bélanger-Quintana A, Burlina A, Harding CO, et…

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Mosaicism

Nov 27, 2016 by in GENERAL & FAMILY MEDICINE Comments Off on Mosaicism

Figure 7-17 Schematic representation of a mutation occurring after conception, during mitotic cell divisions. Such a mutation can lead to a proportion of cells carrying the mutation—that is, to either somatic or…

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References

Nov 27, 2016 by in GENERAL & FAMILY MEDICINE Comments Off on References

General References Campeau PM, Scriver CR, Mitchell JJ. A 25-year longitudinal analysis of treatment efficacy in inborn errors of metabolism. Mol Genet Metab. 2008;95:11–16. Dietz HC. New therapeutic approaches to…

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Problems

Nov 27, 2016 by in GENERAL & FAMILY MEDICINE Comments Off on Problems

-year-old girl, T.N., has been noted to have increasing difficulty standing up after sitting on the floor. Her serum level of creatine kinase is grossly elevated. Although a female, the…

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Pedigrees

Nov 27, 2016 by in GENERAL & FAMILY MEDICINE Comments Off on Pedigrees

Figure 7-2 Symbols commonly used in pedigree charts. Although there is no uniform system of pedigree notation, the symbols used here are according to recent recommendations made by professionals in the field…

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Websites

Nov 27, 2016 by in GENERAL & FAMILY MEDICINE Comments Off on Websites

Useful Websites Mutation Databases Clinical and functional translation of CFTR (CFTR2 project). http://www.cftr2.org/. Collagen mutation database. http://www.le.ac.uk/genetics/collagen/. Cystic fibrosis and CFTR gene mutation database. http://www.gene.sickkids.on.ca/cftr/. Human mitochondrial genome database. http://www.gen.emory.edu/mitomap.html….

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to Specific Topics

Nov 27, 2016 by in GENERAL & FAMILY MEDICINE Comments Off on to Specific Topics

References to Specific Topics Bettens K, Sleegers K, Van Broeckhoven C. Genetic insights in Alzheimer’s disease. Lancet Neurol. 2013;12:92–104. Blau N, Hennermann JB, Langenbeck U, et al. Diagnosis, classification, and…

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