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Medientyp
- Text 6
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Erscheinungsjahr
Autor/in
- Kutsche, Kerstin
- Horn, Denise 2
- Kratz, Christian P 2
- König, Rainer 2
- Mautner, Viktor Felix 2
- alle zeigen
Sprache
- Deutsch 6
6 Einträge gefunden
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Large intragenic deletions of the NF2 gene: breakpoints and associated phenotypes.
2010 - Forschungsinformationssystem des UKE -
A restricted spectrum of NRAS mutations causes Noonan syndrome.
- Cirstea, Ion C
- Kutsche, Kerstin
- Dvorsky, Radovan
- Gremer, Lothar
- Carta, Claudio
- Horn, Denise
- Roberts, Amy E
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The face of Noonan syndrome: Does phenotype predict genotype.
- Allanson, Judith E
- Bohring, Axel
- Dörr, Helmuth-Guenther
- Dufke, Andreas
- Gillessen-Kaesbach, Gabrielle
- Horn, Denise
- König, Rainer
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A severe form of the X-linked microphthalmia with linear skin defects syndrome in a female newborn.
2010 - Forschungsinformationssystem des UKE -