Cat eye syndrome and dystonia
Identifieur interne : 005684 ( Main/Exploration ); précédent : 005683; suivant : 005685Cat eye syndrome and dystonia
Auteurs : Carmelo Nicolosi [Italie] ; Paolo Girlanda [Italie] ; Giuseppe Vita [Italie] ; Corrado Messina [Italie]Source :
- Movement Disorders [ 0885-3185 ] ; 1996-01.
English descriptors
- KwdEn :
- MESH :
- abnormalities : Iris.
- genetics : Chromosome Aberrations, Coloboma, Dystonia.
- Adult, Chromosome Disorders, Chromosomes, Human, Pair 22, Female, Follow-Up Studies, Humans, Neurologic Examination, Syndrome.
Url:
DOI: 10.1002/mds.870110127
Affiliations:
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Le document en format XML
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Disord.</title><idno type="ISSN">0885-3185</idno><idno type="eISSN">1531-8257</idno><imprint><publisher>Wiley Subscription Services, Inc., A Wiley Company</publisher><pubPlace>Hoboken</pubPlace><date type="published" when="1996-01">1996-01</date><biblScope unit="vol">11</biblScope><biblScope unit="issue">1</biblScope><biblScope unit="page" from="110">110</biblScope><biblScope unit="page" to="111">111</biblScope></imprint><idno type="ISSN">0885-3185</idno></series><idno type="istex">A3C6F3808CFD9D1237C911C3215EDCC5C829E8FF</idno><idno type="DOI">10.1002/mds.870110127</idno><idno type="ArticleID">MDS870110127</idno></biblStruct></sourceDesc><seriesStmt><idno type="ISSN">0885-3185</idno></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Adult</term><term>Chromosome Aberrations (genetics)</term><term>Chromosome Disorders</term><term>Chromosomes, Human, Pair 22</term><term>Coloboma (genetics)</term><term>Dystonia (genetics)</term><term>Female</term><term>Follow-Up Studies</term><term>Humans</term><term>Iris (abnormalities)</term><term>Neurologic Examination</term><term>Syndrome</term></keywords><keywords scheme="MESH" qualifier="abnormalities" xml:lang="en"><term>Iris</term></keywords><keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Chromosome Aberrations</term><term>Coloboma</term><term>Dystonia</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Adult</term><term>Chromosome Disorders</term><term>Chromosomes, Human, Pair 22</term><term>Female</term><term>Follow-Up Studies</term><term>Humans</term><term>Neurologic Examination</term><term>Syndrome</term></keywords></textClass><langUsage><language ident="en">en</language></langUsage></profileDesc></teiHeader></TEI><affiliations><list><country><li>Italie</li></country></list><tree><country name="Italie"><noRegion><name sortKey="Nicolosi, Carmelo" sort="Nicolosi, Carmelo" uniqKey="Nicolosi C" first="Carmelo" last="Nicolosi">Carmelo Nicolosi</name></noRegion><name sortKey="Girlanda, Paolo" sort="Girlanda, Paolo" uniqKey="Girlanda P" first="Paolo" last="Girlanda">Paolo Girlanda</name><name sortKey="Messina, Corrado" sort="Messina, Corrado" uniqKey="Messina C" first="Corrado" last="Messina">Corrado Messina</name><name sortKey="Vita, Giuseppe" sort="Vita, Giuseppe" uniqKey="Vita G" first="Giuseppe" last="Vita">Giuseppe Vita</name></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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