Submikroskopiske kromosomanomalier som årsag til skizofreni

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Standard

Submikroskopiske kromosomanomalier som årsag til skizofreni. / Hansen, Thomas; Ingason, Andrés; Werge, Thomas.

I: Ugeskrift for Laeger, Bind 170, Nr. 46, 2008, s. 3773-6.

Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt

Harvard

Hansen, T, Ingason, A & Werge, T 2008, 'Submikroskopiske kromosomanomalier som årsag til skizofreni', Ugeskrift for Laeger, bind 170, nr. 46, s. 3773-6.

APA

Hansen, T., Ingason, A., & Werge, T. (2008). Submikroskopiske kromosomanomalier som årsag til skizofreni. Ugeskrift for Laeger, 170(46), 3773-6.

Vancouver

Hansen T, Ingason A, Werge T. Submikroskopiske kromosomanomalier som årsag til skizofreni. Ugeskrift for Laeger. 2008;170(46):3773-6.

Author

Hansen, Thomas ; Ingason, Andrés ; Werge, Thomas. / Submikroskopiske kromosomanomalier som årsag til skizofreni. I: Ugeskrift for Laeger. 2008 ; Bind 170, Nr. 46. s. 3773-6.

Bibtex

@article{a78c07af55854035b8d3bd73321bd27d,
title = "Submikroskopiske kromosomanomalier som {\aa}rsag til skizofreni",
abstract = "Although the inheritable nature of schizophrenia is well-established, the genetic underpinnings remain largely hidden. Recently, two independent research groups identified microdeletions conferring high risk of schizophrenia. The deletions are recurrent in nature and offer an explanation to the apparently stable prevalence of the disease, despite reduced fecundity in patients. The findings may lead to development of diagnostic tools and construction of new disease models to help the development of novel therapeutic strategies.",
author = "Thomas Hansen and Andr{\'e}s Ingason and Thomas Werge",
year = "2008",
language = "Dansk",
volume = "170",
pages = "3773--6",
journal = "Ugeskrift for Laeger",
issn = "0041-5782",
publisher = "Almindelige Danske Laegeforening",
number = "46",

}

RIS

TY - JOUR

T1 - Submikroskopiske kromosomanomalier som årsag til skizofreni

AU - Hansen, Thomas

AU - Ingason, Andrés

AU - Werge, Thomas

PY - 2008

Y1 - 2008

N2 - Although the inheritable nature of schizophrenia is well-established, the genetic underpinnings remain largely hidden. Recently, two independent research groups identified microdeletions conferring high risk of schizophrenia. The deletions are recurrent in nature and offer an explanation to the apparently stable prevalence of the disease, despite reduced fecundity in patients. The findings may lead to development of diagnostic tools and construction of new disease models to help the development of novel therapeutic strategies.

AB - Although the inheritable nature of schizophrenia is well-established, the genetic underpinnings remain largely hidden. Recently, two independent research groups identified microdeletions conferring high risk of schizophrenia. The deletions are recurrent in nature and offer an explanation to the apparently stable prevalence of the disease, despite reduced fecundity in patients. The findings may lead to development of diagnostic tools and construction of new disease models to help the development of novel therapeutic strategies.

M3 - Tidsskriftartikel

VL - 170

SP - 3773

EP - 3776

JO - Ugeskrift for Laeger

JF - Ugeskrift for Laeger

SN - 0041-5782

IS - 46

ER -

ID: 48610787