@prefix ns1: .
@prefix rdf: .
@prefix rdfs: .
@prefix schema: .
@prefix skos: .
@prefix xml: .
@prefix xsd: .
schema:name "Laitinen, Eeva-Maria" .
a ,
schema:CreativeWork ;
ns1:P60048 ;
ns1:P60050 ;
schema:datePublished "2012" ;
schema:description "Artikkeliväitöskirjan yhteenveto-osa ja 5 eripainosta.",
"Nimiösivulla myös: National Graduate School of Clinical Investigation, Pediatric Graduate School, Children's Hospital, Institute of Clinical Medicine and Institute of Biomedicine/Physiology, University of Helsinki, Helsinki, Finland.",
"kuvitettu" ;
schema:exampleOfWork ;
schema:identifier [ a schema:PropertyValue ;
schema:propertyID "FI-MELINDA" ;
schema:value "006030381" ],
[ a schema:PropertyValue ;
schema:propertyID "skl" ;
schema:value "fx996643" ],
[ a schema:PropertyValue ;
schema:propertyID "FI-FENNI" ;
schema:value "996643" ] ;
schema:isPartOf ;
schema:isbn "9789521081323" ;
schema:name "Kallmann syndrome : clinical and molecular genetic features in Finland" ;
schema:numberOfPages "94, [37] sivu" ;
schema:publication [ schema:location [ schema:name "Helsinki" ] ;
schema:organizer ] ;
schema:publisher .
a ,
schema:CreativeWork ;
schema:description "Yhteenveto-osa julkaistu myös verkkoaineistona ISBN 978-952-10-8133-0 (PDF)" ;
schema:exampleOfWork ;
schema:isPartOf ;
schema:name "Kallmann syndrome : clinical and molecular genetic features in Finland" .
a ,
schema:Book,
schema:CreativeWork ;
schema:bookFormat schema:EBook ;
schema:exampleOfWork ;
schema:isPartOf ;
schema:name "Kallmann syndrome : clinical and molecular genetic features in Finland" ;
schema:url .
a ,
schema:Book,
schema:CreativeWork ;
ns1:P60048 ;
ns1:P60050 ;
schema:bookFormat schema:EBook ;
schema:datePublished "2012" ;
schema:description "Artikkeliväitöskirjan yhteenveto-osa.",
"Nimeke PDF-nimiönäytöstä.",
"Nimiösivulla myös: National Graduate School of Clinical Investigation, Pediatric Graduate School, Children's Hospital, Institute of Clinical Medicine and Institute of Biomedicine/Physiology, University of Helsinki, Helsinki, Finland." ;
schema:exampleOfWork ;
schema:identifier [ a schema:PropertyValue ;
schema:propertyID "FI-MELINDA" ;
schema:value "006030382" ],
[ a schema:PropertyValue ;
schema:propertyID "skl" ;
schema:value "fx1002023" ],
[ a schema:PropertyValue ;
schema:propertyID "FI-FENNI" ;
schema:value "1002023" ] ;
schema:isPartOf ;
schema:isbn "9789521081330" ;
schema:name "Kallmann syndrome : clinical and molecular genetic features in Finland" ;
schema:numberOfPages "1 PDF-tiedosto (94 s.)" ;
schema:publication [ schema:location [ schema:name "Helsinki" ] ;
schema:organizer ] ;
schema:publisher ;
schema:url [ ],
[ ] .
a ,
schema:CreativeWork ;
schema:description "Julkaistu myös painettuna ISBN 978-952-10-8132-3" ;
schema:exampleOfWork ;
schema:isPartOf ;
schema:name "Kallmann syndrome : clinical and molecular genetic features in Finland" .
schema:name "hypogonadotrooppinen hypogonadismi" .
schema:name "Kallmannin oireyhtymä" .
schema:name "Helsingin yliopisto" .
a ,
schema:CreativeWork ;
ns1:P60049 ;
schema:about ,
;
schema:author ;
schema:inLanguage "en" ;
schema:isPartOf ;
schema:name "Kallmann syndrome : clinical and molecular genetic features in Finland" ;
schema:workExample ,
,
,
,
.
schema:name "Fennica" .