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Angaben zur Quelle [Bearbeiten]

Autor     Nicholas J Neill, Beth S Torchia, Bassem A Bejjani, Lisa G Shaffer, Blake C Ballif
Titel    Comparative analysis of copy number detection by whole-genome BAC and oligonucleotide

array CGH

Zeitschrift    Molecular Cytogenetics
Ausgabe    3
Datum    29. June 2010
Nummer    11
Seiten    1-14
Anmerkung    PubMed ID: 20587050
DOI    10.1186/1755-8166-3-11
URL    http://www.molecularcytogenetics.org/content/3/1/11

Literaturverz.   

yes
Fußnoten    yes
Fragmente    1


Fragmente der Quelle:
[1.] Mmu/Fragment 010 10b - Diskussion
Zuletzt bearbeitet: 2014-12-22 15:36:00 Hindemith
BauernOpfer, Fragment, Gesichtet, Mmu, Neill et al 2010, SMWFragment, Schutzlevel sysop

Typus
BauernOpfer
Bearbeiter
Graf Isolan
Gesichtet
Yes.png
Untersuchte Arbeit:
Seite: 10, Zeilen: 10-15
Quelle: Neill et al 2010
Seite(n): 1 (electronic version), Zeilen: right col. 3-12
Therefore, the application of aCGH has created a paradigm shift in genetics that has moved the description and discovery of genetic conditions from the "phenotype-first" approach, in which patients exhibiting similar clinical features are identified prior to the discovery of an underlying aetiology, to a "genotype-first" approach, in which a collection of individuals with similar copy-number imbalances can be examined for common clinical features (Neill 2010).

56. Neill N.J., et al., Comparative analysis of copy number detection by whole-genome BAC and oligonucleotide array CGH. Mol Cytogenet, 2010. 3: p. 11.

Furthermore, the application of aCGH has created a paradigm shift in genetics that has moved the description and discovery of genetic conditions from the “phenotype-first”

approach, in which patients exhibiting similar clinical features are identified prior to the discovery of an underlying etiology, to a “genotype-first” approach, in which a collection of individuals with similar copy-number imbalances can be examined for common clinical features [15].


15. Shaffer LG, Theisen A, Bejjani BA, Ballif BC, Aylsworth AS, Lim C, McDonald M, Ellison JW, Kostiner D, Saitta S, Shaikh T: The discovery of microdeletion syndromes in the post-genomic era: review of the methodology and characterization of a new 1q41q42 microdeletion syndrome. Genet Med 2007, 9:607-616.

Anmerkungen

Although nearly identical, nothing has been marked as a citation. Since the reference has been changed to Neill 2010, it is more probable that this piece has been taken from Papa 2010 (see Mmu/Fragment_010_10).

Sichter
(Graf Isolan), SleepyHollow02

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