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pro vyhledávání: '"Herman E. Wyandt"'
This new edition now titled “Human Chromosome Variation: Heteromorphism, Polymorphism and Pathogenesis” provides the reader with an up-to-date overview of microarrays, fragile sites, copy number variations and whole genome sequencing. Greatly exp
Publikováno v:
Human Chromosome Variation: Heteromorphism, Polymorphism and Pathogenesis ISBN: 9789811030345
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7a6d12d7ac8bb9c6a20d644c0370ea5d
https://doi.org/10.1007/978-981-10-3035-2_4
https://doi.org/10.1007/978-981-10-3035-2_4
Publikováno v:
Human Chromosome Variation: Heteromorphism, Polymorphism and Pathogenesis ISBN: 9789811030345
Two revolutionary advances in molecular biology have enabled scanning of the entire human genome for genetic variation: 1. Array-comparative genomic hybridization-microarray analysis (aCGH, CMA, microarray analysis, referred to henceforth as aCGH) th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::15fd4f41ffaf1f4ed933f80e647992a4
https://doi.org/10.1007/978-981-10-3035-2_9
https://doi.org/10.1007/978-981-10-3035-2_9
Publikováno v:
Human Chromosome Variation: Heteromorphism, Polymorphism and Pathogenesis ISBN: 9789811030345
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f7f10d0dc79126e684bdb42e7ae6f948
https://doi.org/10.1007/978-981-10-3035-2_1
https://doi.org/10.1007/978-981-10-3035-2_1
Publikováno v:
Human Chromosome Variation: Heteromorphism, Polymorphism and Pathogenesis ISBN: 9789811030345
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::433dfad00dd6fd740149e4a9fb323dbb
https://doi.org/10.1007/978-981-10-3035-2_3
https://doi.org/10.1007/978-981-10-3035-2_3
Publikováno v:
Human Chromosome Variation: Heteromorphism, Polymorphism and Pathogenesis ISBN: 9789811030345
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3bc2eb108d4a66bcc8cdcbc4e8f2341d
https://doi.org/10.1007/978-981-10-3035-2_7
https://doi.org/10.1007/978-981-10-3035-2_7
Publikováno v:
Human Chromosome Variation: Heteromorphism, Polymorphism and Pathogenesis ISBN: 9789811030345
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7d547c34fef8502e2e16e4b99352393a
https://doi.org/10.1007/978-981-10-3035-2_2
https://doi.org/10.1007/978-981-10-3035-2_2
Publikováno v:
Human Chromosome Variation: Heteromorphism, Polymorphism and Pathogenesis ISBN: 9789811030345
Discussion of DNA diagnosis using targeted DNA or whole exome sequencine (WES) is necessarily truncated because of two reasons.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a1a09637b8ac8081c71b5e0104ebf951
https://doi.org/10.1007/978-981-10-3035-2_11
https://doi.org/10.1007/978-981-10-3035-2_11
Publikováno v:
Human Chromosome Variation: Heteromorphism, Polymorphism and Pathogenesis ISBN: 9789811030345
Rapid incorporation of microarray analysis/aCGH for studies of children with developmental disabilities and its endorsement as a first-tier test for these children [1] has yielded a vast number of subtle chromosome changes that were unseen by routine
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b8036fa497e6aa6318639a4134e03586
https://doi.org/10.1007/978-981-10-3035-2_10
https://doi.org/10.1007/978-981-10-3035-2_10