Serveur d'exploration sur la musique celtique

Attention, ce site est en cours de développement !
Attention, site généré par des moyens informatiques à partir de corpus bruts.
Les informations ne sont donc pas validées.

Genetic and clinical heterogeneity in tapetal retinal dystrophies

Identifieur interne : 000D08 ( Main/Exploration ); précédent : 000D07; suivant : 000D09

Genetic and clinical heterogeneity in tapetal retinal dystrophies

Auteurs : A. A. B. Bergen [Pays-Bas]

Source :

RBID : ISTEX:548672778DC2F17360CC1B3234B9919C4E23704B

Abstract

Large scale DNA-mutation screening in patients with hereditary retinal diseases greatly enhances our knowledge about retinal function and diseases. Scientists, clinicians, patients, and families involved with retinal disorders may directly benefit from these developments. However, certain aspects of this expanding knowledge, such as the correlation between genotype and phenotype, may be much more complicated than we expect at present.

Url:
DOI: 10.1017/S0140525X0003925X


Affiliations:


Links toward previous steps (curation, corpus...)


Le document en format XML

<record>
<TEI wicri:istexFullTextTei="biblStruct">
<teiHeader>
<fileDesc>
<titleStmt>
<title>Genetic and clinical heterogeneity in tapetal retinal dystrophies</title>
<author>
<name sortKey="Bergen, A A B" sort="Bergen, A A B" uniqKey="Bergen A" first="A. A. B." last="Bergen">A. A. B. Bergen</name>
</author>
</titleStmt>
<publicationStmt>
<idno type="wicri:source">ISTEX</idno>
<idno type="RBID">ISTEX:548672778DC2F17360CC1B3234B9919C4E23704B</idno>
<date when="1995" year="1995">1995</date>
<idno type="doi">10.1017/S0140525X0003925X</idno>
<idno type="url">https://api.istex.fr/document/548672778DC2F17360CC1B3234B9919C4E23704B/fulltext/pdf</idno>
<idno type="wicri:Area/Istex/Corpus">002007</idno>
<idno type="wicri:explorRef" wicri:stream="Istex" wicri:step="Corpus" wicri:corpus="ISTEX">002007</idno>
<idno type="wicri:Area/Istex/Curation">001248</idno>
<idno type="wicri:Area/Istex/Checkpoint">000A69</idno>
<idno type="wicri:explorRef" wicri:stream="Istex" wicri:step="Checkpoint">000A69</idno>
<idno type="wicri:doubleKey">0140-525X:1995:Bergen A:genetic:and:clinical</idno>
<idno type="wicri:Area/Main/Merge">000D11</idno>
<idno type="wicri:Area/Main/Curation">000D08</idno>
<idno type="wicri:Area/Main/Exploration">000D08</idno>
</publicationStmt>
<sourceDesc>
<biblStruct>
<analytic>
<title level="a">Genetic and clinical heterogeneity in tapetal retinal dystrophies</title>
<author>
<name sortKey="Bergen, A A B" sort="Bergen, A A B" uniqKey="Bergen A" first="A. A. B." last="Bergen">A. A. B. Bergen</name>
<affiliation wicri:level="1">
<country wicri:rule="url">Pays-Bas</country>
<wicri:regionArea>The Netherlands Ophthalmic Research Institute, 1100 AC Amsterdam, The Netherlands</wicri:regionArea>
<wicri:noRegion>The Netherlands</wicri:noRegion>
</affiliation>
</author>
</analytic>
<monogr></monogr>
<series>
<title level="j">Behavioral and Brain Sciences</title>
<title level="j" type="abbrev">Behav Brain Sci</title>
<idno type="ISSN">0140-525X</idno>
<idno type="eISSN">1469-1825</idno>
<imprint>
<publisher>Cambridge University Press</publisher>
<pubPlace>Cambridge, UK</pubPlace>
<date type="published" when="1995-09">1995-09</date>
<biblScope unit="volume">18</biblScope>
<biblScope unit="issue">3</biblScope>
<biblScope unit="page" from="470">470</biblScope>
<biblScope unit="page" to="471">471</biblScope>
</imprint>
<idno type="ISSN">0140-525X</idno>
</series>
</biblStruct>
</sourceDesc>
<seriesStmt>
<idno type="ISSN">0140-525X</idno>
</seriesStmt>
</fileDesc>
<profileDesc>
<textClass></textClass>
<langUsage>
<language ident="en">en</language>
</langUsage>
</profileDesc>
</teiHeader>
<front>
<div type="abstract">Large scale DNA-mutation screening in patients with hereditary retinal diseases greatly enhances our knowledge about retinal function and diseases. Scientists, clinicians, patients, and families involved with retinal disorders may directly benefit from these developments. However, certain aspects of this expanding knowledge, such as the correlation between genotype and phenotype, may be much more complicated than we expect at present.</div>
</front>
</TEI>
<affiliations>
<list>
<country>
<li>Pays-Bas</li>
</country>
</list>
<tree>
<country name="Pays-Bas">
<noRegion>
<name sortKey="Bergen, A A B" sort="Bergen, A A B" uniqKey="Bergen A" first="A. A. B." last="Bergen">A. A. B. Bergen</name>
</noRegion>
</country>
</tree>
</affiliations>
</record>

Pour manipuler ce document sous Unix (Dilib)

EXPLOR_STEP=$WICRI_ROOT/Wicri/Musique/explor/MusiqueCeltiqueV1/Data/Main/Exploration
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 000D08 | SxmlIndent | more

Ou

HfdSelect -h $EXPLOR_AREA/Data/Main/Exploration/biblio.hfd -nk 000D08 | SxmlIndent | more

Pour mettre un lien sur cette page dans le réseau Wicri

{{Explor lien
   |wiki=    Wicri/Musique
   |area=    MusiqueCeltiqueV1
   |flux=    Main
   |étape=   Exploration
   |type=    RBID
   |clé=     ISTEX:548672778DC2F17360CC1B3234B9919C4E23704B
   |texte=   Genetic and clinical heterogeneity in tapetal retinal dystrophies
}}

Wicri

This area was generated with Dilib version V0.6.38.
Data generation: Sat May 29 22:04:25 2021. Site generation: Sat May 29 22:08:31 2021