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Autor/in
- Orth, Ulrike
- Gal, Andreas 5
- Kutsche, Kerstin 2
- Rau, Isabella 2
- Azam, Maleeha 1
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- Deutsch 7
7 Einträge gefunden
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[Hereditary cardiac amyloidosis with transthyretin mutations. A cause of sudden death ].
2012 - Forschungsinformationssystem des UKE -
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A homozygous p.Glu150Lys mutation in the opsin gene of two Pakistani families with autosomal recessive retinitis pigmentosa.
- Azam, Maleeha
- Khan, Muhammad Imran
- Gal, Andreas
- Hussain, Alamdar
- Shah, Syed Tahir Abbas
- Khan, Muhammad Shakil
- Sadeque, Ahmed
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[Mutations of the frizzled-4 gene. Their impact on medical care of patients with autosomal dominant exudative vitreoretinopathy]
2008 - Forschungsinformationssystem des UKE -
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Seventeen novel PLP1 mutations in patients with Pelizaeus-Merzbacher disease.
- Hübner, Christian A
- Orth, Ulrike
- Senning, Arne
- Steglich, Cordula
- Kohlschütter, Alfried
- Korinthenberg, Rudolf
- Gal, Andreas