Congenital profound sensorineural deafness and oligodontia: a new syndrome.
Identifieur interne : 006091 ( PubMed/Corpus ); précédent : 006090; suivant : 006092Congenital profound sensorineural deafness and oligodontia: a new syndrome.
Auteurs : L. Glass ; R J GorlinSource :
- Archives of otolaryngology (Chicago, Ill. : 1960) [ 0003-9977 ] ; 1979.
English descriptors
- KwdEn :
- MESH :
- congenital : Hearing Loss, Sensorineural.
- diagnostic imaging : Dentition, Mixed, Jaw, Edentulous, Partially.
- genetics : Hearing Loss, Sensorineural, Tooth Abnormalities.
- Child, Female, Genes, Recessive, Humans, Male, Radiography, Syndrome.
PubMed: 485932
Links to Exploration step
pubmed:485932Le document en format XML
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<author><name sortKey="Glass, L" sort="Glass, L" uniqKey="Glass L" first="L" last="Glass">L. Glass</name>
</author>
<author><name sortKey="Gorlin, R J" sort="Gorlin, R J" uniqKey="Gorlin R" first="R J" last="Gorlin">R J Gorlin</name>
</author>
</titleStmt>
<publicationStmt><idno type="wicri:source">PubMed</idno>
<date when="1979">1979</date>
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<sourceDesc><biblStruct><analytic><title xml:lang="en">Congenital profound sensorineural deafness and oligodontia: a new syndrome.</title>
<author><name sortKey="Glass, L" sort="Glass, L" uniqKey="Glass L" first="L" last="Glass">L. Glass</name>
</author>
<author><name sortKey="Gorlin, R J" sort="Gorlin, R J" uniqKey="Gorlin R" first="R J" last="Gorlin">R J Gorlin</name>
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<series><title level="j">Archives of otolaryngology (Chicago, Ill. : 1960)</title>
<idno type="ISSN">0003-9977</idno>
<imprint><date when="1979" type="published">1979</date>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Child</term>
<term>Dentition, Mixed (diagnostic imaging)</term>
<term>Female</term>
<term>Genes, Recessive</term>
<term>Hearing Loss, Sensorineural (congenital)</term>
<term>Hearing Loss, Sensorineural (genetics)</term>
<term>Humans</term>
<term>Jaw, Edentulous, Partially (diagnostic imaging)</term>
<term>Male</term>
<term>Radiography</term>
<term>Syndrome</term>
<term>Tooth Abnormalities (genetics)</term>
</keywords>
<keywords scheme="MESH" qualifier="congenital" xml:lang="en"><term>Hearing Loss, Sensorineural</term>
</keywords>
<keywords scheme="MESH" qualifier="diagnostic imaging" xml:lang="en"><term>Dentition, Mixed</term>
<term>Jaw, Edentulous, Partially</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Hearing Loss, Sensorineural</term>
<term>Tooth Abnormalities</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Child</term>
<term>Female</term>
<term>Genes, Recessive</term>
<term>Humans</term>
<term>Male</term>
<term>Radiography</term>
<term>Syndrome</term>
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<pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">485932</PMID>
<DateCompleted><Year>1979</Year>
<Month>11</Month>
<Day>29</Day>
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<DateRevised><Year>2016</Year>
<Month>11</Month>
<Day>23</Day>
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<Article PubModel="Print"><Journal><ISSN IssnType="Print">0003-9977</ISSN>
<JournalIssue CitedMedium="Print"><Volume>105</Volume>
<Issue>10</Issue>
<PubDate><Year>1979</Year>
<Month>Oct</Month>
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<Title>Archives of otolaryngology (Chicago, Ill. : 1960)</Title>
<ISOAbbreviation>Arch Otolaryngol</ISOAbbreviation>
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<ArticleTitle>Congenital profound sensorineural deafness and oligodontia: a new syndrome.</ArticleTitle>
<Pagination><MedlinePgn>621-2</MedlinePgn>
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<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Glass</LastName>
<ForeName>L</ForeName>
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<Author ValidYN="Y"><LastName>Gorlin</LastName>
<ForeName>R J</ForeName>
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<Language>eng</Language>
<PublicationTypeList><PublicationType UI="D002363">Case Reports</PublicationType>
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<MedlineJournalInfo><Country>United States</Country>
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<MeshHeadingList><MeshHeading><DescriptorName UI="D002648" MajorTopicYN="N">Child</DescriptorName>
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<MeshHeading><DescriptorName UI="D005260" MajorTopicYN="N">Female</DescriptorName>
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<MeshHeading><DescriptorName UI="D005808" MajorTopicYN="N">Genes, Recessive</DescriptorName>
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<MeshHeading><DescriptorName UI="D006319" MajorTopicYN="N">Hearing Loss, Sensorineural</DescriptorName>
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<QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D006801" MajorTopicYN="N">Humans</DescriptorName>
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<MeshHeading><DescriptorName UI="D013577" MajorTopicYN="N">Syndrome</DescriptorName>
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<MeshHeading><DescriptorName UI="D014071" MajorTopicYN="N">Tooth Abnormalities</DescriptorName>
<QualifierName UI="Q000235" MajorTopicYN="Y">genetics</QualifierName>
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