Genetik Hastalıklar İçin Kullanılan Tanı Testleri
Özet
Referanslar
Gardner RM, Sutherland GR, Shaffer LG. Chromosome abnormalities and genetic counseling: OUP USA; 2012.
Nussbaum RL, McInnes RR, Willard HF. Thompson & Thompson Genetics in Medicine E-Book: Thompson & Thompson Genetics in Medicine E-Book: Elsevier Health Sciences; 2015.
Berisha SZ, Shetty S, Prior TW, Mitchell AL. Cytogenetic and molecular diagnostic testing associated with prenatal and postnatal birth defects. Birth defects research. 2020;112(4):293-306.
Haaf TMeyers R. Fluorescence in situ hybridization. Encyclopedia of analytic chemistry. Chichester, UK: John Wiley & sons Ltd; 2000.
Lucito R, Healy J, Alexander J, Reiner A, Esposito D, Chi M, et al. Representational oligonucleotide microarray analysis: a high-resolution method to detect genome copy number variation. Genome research. 2003;13(10):2291-305.
DeRisi J, Penland L, Bittner M, Meltzer P, Ray M, Chen Y, et al. Use of a cDNA microarray to analyse gene expression. Nat genet. 1996;14:457-60.
Schena M, Shalon D, Davis RW, Brown PO. Quantitative monitoring of gene expression patterns with a complementary DNA microarray. Science. 1995;270(5235):467-70.
Schochetman G, Ou C-Y, Jones WK. Polymerase chain reaction. The Journal of infectious diseases. 1988;158(6):1154-7.
Chamberlain JS, Gibbs RA, Rainer JE, Nguyen PN, Thomas C. Deletion screening of the Duchenne muscular dystrophy locus via multiplex DNA amplification. Nucleic acids research. 1988;16(23):11141-56.
Sanger F, Coulson AR. A rapid method for determining sequences in DNA by primed synthesis with DNA polymerase. Journal of molecular biology. 1975;94(3):441-8.
Bleidorn C. Third generation sequencing: technology and its potential impact on evolutionary biodiversity research. Systematics and biodiversity. 2016;14(1):1-8.
Referanslar
Gardner RM, Sutherland GR, Shaffer LG. Chromosome abnormalities and genetic counseling: OUP USA; 2012.
Nussbaum RL, McInnes RR, Willard HF. Thompson & Thompson Genetics in Medicine E-Book: Thompson & Thompson Genetics in Medicine E-Book: Elsevier Health Sciences; 2015.
Berisha SZ, Shetty S, Prior TW, Mitchell AL. Cytogenetic and molecular diagnostic testing associated with prenatal and postnatal birth defects. Birth defects research. 2020;112(4):293-306.
Haaf TMeyers R. Fluorescence in situ hybridization. Encyclopedia of analytic chemistry. Chichester, UK: John Wiley & sons Ltd; 2000.
Lucito R, Healy J, Alexander J, Reiner A, Esposito D, Chi M, et al. Representational oligonucleotide microarray analysis: a high-resolution method to detect genome copy number variation. Genome research. 2003;13(10):2291-305.
DeRisi J, Penland L, Bittner M, Meltzer P, Ray M, Chen Y, et al. Use of a cDNA microarray to analyse gene expression. Nat genet. 1996;14:457-60.
Schena M, Shalon D, Davis RW, Brown PO. Quantitative monitoring of gene expression patterns with a complementary DNA microarray. Science. 1995;270(5235):467-70.
Schochetman G, Ou C-Y, Jones WK. Polymerase chain reaction. The Journal of infectious diseases. 1988;158(6):1154-7.
Chamberlain JS, Gibbs RA, Rainer JE, Nguyen PN, Thomas C. Deletion screening of the Duchenne muscular dystrophy locus via multiplex DNA amplification. Nucleic acids research. 1988;16(23):11141-56.
Sanger F, Coulson AR. A rapid method for determining sequences in DNA by primed synthesis with DNA polymerase. Journal of molecular biology. 1975;94(3):441-8.
Bleidorn C. Third generation sequencing: technology and its potential impact on evolutionary biodiversity research. Systematics and biodiversity. 2016;14(1):1-8.
