References

1. Cowell, J.K. Somatic Cell Hybrids in the Analysis of the 9. Human Genome. In Human Cytogenetics, A Practical Approach, 2nd Ed.; Rooney, D.E., Czepulkowski, B.H.,

Eds.; Oxford University Press: Oxford, 1992; 235-292.

2. Papadopoulos, N.; Leach, F.S.; Kinzler, K.W.; Vogelstein, B. Monoallelic mutation analysis (MAMA) for identifying germline mutations. Nat. Genet. 1995, 11 (9), 99-102.

3. Yan, H.; Papadopoulos, N.; Marra, G.; Perrera, C.; Jiricny,

J.; Boland, C.R.; Lynch, H.T.; Chadwick, R.B.; de la 10. Chapelle, A.; Berg, K.; Eshleman, J.R.; Yuan, W.; Markowitz, S.; Laken, S.J.; Lengauer, C.; Kinzler, K.W.; Vogelstein, B. Conversion of diploidy to haploidy. Nature 2000, 403, 723 -724.

4. Nakagawa, H.; Yan, H.; Lockman, J.; Hampel, H.; Kinzler, 11. K.W.; Vogelstein, B.; de la Chapelle, A. Allele separation facilitates interpretation of potential splicing alterations and genomic rearrangements. Cancer Res. 2002, 62, 12. 4579-4582.

5. Monk, D.; Bentley, L.; Hitchins, M.; Myler, R.A.; Clayton-

Smith, J.; Ismail, S.; Price, S.M.; Preece, M.A.; Stanier, 13. P.; Moore, G.E. Chromosome 7p disruptions in Silver Russell Syndrome: Delineating an imprinted candidate gene region. Hum. Genet. 2002, 111, 376-387. 14.

6. Mcdaniel, L.D.; Legerski, R.; Lehmann, A.R.; Freidberg, E.C.; Schultz, R.A. Confirmation of homozygosity for a single nucleotide substitution mutation in a Cockayne Syndrome patient using monoallelic mutation analysis in somatic cell hybrids. Hum. Mutat. 1997, 10, 317-321. 15.

7. Kitamura, E.; Kuemerle, B.A.; Chernova, O.B.; Cowell, J.K. Molecular characterization of the breakpoint region associated with a constitutional t(2;15)(q34;q26) in a patient with multiple myeloma. Cancer Genet. Cytogenet. 2001, 129, 112-119.

Pyatt, R.E.; Nakagawa, H.; Sedra, M.; Fuchik, M.B.; Comeras, I.; de al Chapelle, A.; Prior, T.W. Identification of a deletion in the mismatch repair gene, MSH2, using mouse-human cell hybrids monosomal for chromosome 2. Clin. Genet. 2003, 63, 215 -218.

Mailman, M.D.; Hemingway, T.; Darsey, R.L.; Glasure, C.E.; Huang, Y.; Chadwick, R.B.; Heinz, J.W.; Papp, A.C.; Snyder, P.J.; Sedra, M.S.; Schafer, R.W.; Abuelo, D.N.; Reich, E.W.; Theil, K.S.; Burghes, A.H.M.; de la Chapelle, A.; Prior, T.W. Hybrids monosomal for human chromosome 5 reveal the presence of a spinal muscular atrophy (SMA) carrier with two SMN! Copies on one chromosome. Hum. Genet. 2001, 108, 109-115. Bandyopadhyay, R.; McCaskill, C.; Knox-Du Bois, C.; Zhou, Y.; Berend, S.A.; Bijlsma, E.; Shaffer, L.G. Mosaicism in a patient with Down Syndrome reveals post-fertilization formation of a Robertsonian translocation and isochromosome. Am. J. Hum. Genet. 2003, 116A, 159-163. Patterson, D.; Jones, C.; Scoggin, C.; Miller, Y.E.; Graw, S. Somatic cell genetic approaches to Down's Syndrome. Ann. N.Y. Acad. Sci. 1982, 396, 69-81. Shen, J.J.; Sherman, S.L.; Hassold, T.J. Centromeric genotyping and direct analysis of nondisjunction in humans: Down syndrome. Chromosoma 1998, 107, 166-172. Lynch, H.T.; de la Chapelle, A. Genetic susceptibility to non-polyposis colorectal cancer. J. Med. Genet. 1999, 36, 801-818.

McAndrew, P.E.; Parsons, D.W.; Simard, L.R.; Rochette, C.; Ray, P.N.; Mendell, J.R.; Prior, T.W. Identification of proximal spinal muscular atrophy carriers and patients by analysis of SMNT and SMNC gene copy number. Am. J. Hum. Genet. 1997, 60, 1411-1422. Matsui, S.I.; Faitar, S.J.; Rossi, M.R.; Cowell, J.K. Application of spectral karyotyping to the analysis of human chromosome complement of interspecies somatic cell hybrids. Cancer Genet. Cytogenet. 2003, 142, 30-35.

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