Kallmann syndrome : clinical and molecular genetic features in Finland

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  • en
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  • Kallmann syndrome : clinical and molecular genetic features in Finland
P60049

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Kallmann syndrome : clinical and molecular genetic features in Finland

description
  • Yhteenveto-osa julkaistu myös verkkoaineistona ISBN 978-952-10-8133-0 (PDF)
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name
  • Kallmann syndrome : clinical and molecular genetic features in Finland

Kallmann syndrome : clinical and molecular genetic features in Finland

description
  • Julkaistu myös painettuna ISBN 978-952-10-8132-3
isPartOf
name
  • Kallmann syndrome : clinical and molecular genetic features in Finland

Kallmann syndrome : clinical and molecular genetic features in Finland

bookFormat
isPartOf
name
  • Kallmann syndrome : clinical and molecular genetic features in Finland
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Kallmann syndrome : clinical and molecular genetic features in Finland

datePublished
  • 2012
description
  • Artikkeliväitöskirjan yhteenveto-osa ja 5 eripainosta.
  • kuvitettu
  • 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.
identifier
  • propertyID: FI-FENNI value: 996643
  • propertyID: FI-MELINDA value: 006030381
  • propertyID: skl value: fx996643
isbn
  • 9789521081323
isPartOf
name
  • Kallmann syndrome : clinical and molecular genetic features in Finland
numberOfPages
  • 94, [37] sivu
P60048
P60050
publication
  • location: Helsinki organizer: Helsingin yliopisto
publisher

Kallmann syndrome : clinical and molecular genetic features in Finland

bookFormat
datePublished
  • 2012
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.
identifier
  • propertyID: FI-FENNI value: 1002023
  • propertyID: FI-MELINDA value: 006030382
  • propertyID: skl value: fx1002023
isbn
  • 9789521081330
isPartOf
name
  • Kallmann syndrome : clinical and molecular genetic features in Finland
numberOfPages
  • 1 PDF-tiedosto (94 s.)
P60048
P60050
publication
  • location: Helsinki organizer: Helsingin yliopisto
publisher
url

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