Prader-Willi syndrome due to uniparental disomy in a patient with a balanced chromosomal translocation

Result code in IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11130%2F06%3A180" target="_blank" >RIV/00216208:11130/06:180 - isvavai.cz</a>

Result on the web

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DOI - Digital Object Identifier

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Result language

angličtina

Original language name

Prader-Willi syndrome due to uniparental disomy in a patient with a balanced chromosomal translocation

Original language description

OBJECTIVES: In contrast to most human autosomal genes which are expressed biallelically, the expression of imprinted genes depends on the parental origin of the allele. Prader-Willi syndrome is a neurobehavioral disorder in which the expression of active

Czech name

Prader Willi syndrome due to uniparental disomy in a patient with a balanced chromosomal translocation

Czech description

OBJECTIVES - In contrast to most human autosomal genes which are expressed biallelically, the expression of imprinted genes depends on the parental origin of the allele. Prader-Willi syndrome is a neurobehavioral disorder in which the expression of activ

Type

J_x - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

CEP classification

EB - Genetics and molecular biology

OECD FORD branch

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Project

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Continuities

Z - Vyzkumny zamer (s odkazem do CEZ)

Publication year

2006

Confidentiality

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Name of the periodical

Neuroendocrinology letters

ISSN

0172-780X

e-ISSN

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Volume of the periodical

27

Issue of the periodical within the volume

5

Country of publishing house

SE - SWEDEN

Number of pages

7

Pages from-to

579-585

UT code for WoS article

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EID of the result in the Scopus database

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