Expanded newborn screening: Long term follow up of 25 patients with organic acidemias and urea cycle disorders

Trefz FK, Töpel T, Scheible D, Frauendienst-Egger G, Hofestädt R (2006)
JOURNAL OF INHERITED METABOLIC DISEASE 29(Suppl. 1): 84.

Kurzbeitrag Konferenz / Poster | Veröffentlicht | Englisch
 
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Autor*in
Trefz, F. K.; Töpel, ThoralfUniBi; Scheible, D.; Frauendienst-Egger, G.; Hofestädt, RalfUniBi
Erscheinungsjahr
2006
Band
29
Ausgabe
Suppl. 1
Seite(n)
84
ISSN
0141-8955
Page URI
https://pub.uni-bielefeld.de/record/1596361

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Trefz FK, Töpel T, Scheible D, Frauendienst-Egger G, Hofestädt R. Expanded newborn screening: Long term follow up of 25 patients with organic acidemias and urea cycle disorders. JOURNAL OF INHERITED METABOLIC DISEASE. 2006;29(Suppl. 1):84.
Trefz, F. K., Töpel, T., Scheible, D., Frauendienst-Egger, G., & Hofestädt, R. (2006). Expanded newborn screening: Long term follow up of 25 patients with organic acidemias and urea cycle disorders. JOURNAL OF INHERITED METABOLIC DISEASE, 29(Suppl. 1), 84.
Trefz, F. K., Töpel, T., Scheible, D., Frauendienst-Egger, G., and Hofestädt, R. (2006). Expanded newborn screening: Long term follow up of 25 patients with organic acidemias and urea cycle disorders. JOURNAL OF INHERITED METABOLIC DISEASE 29, 84.
Trefz, F.K., et al., 2006. Expanded newborn screening: Long term follow up of 25 patients with organic acidemias and urea cycle disorders. JOURNAL OF INHERITED METABOLIC DISEASE, 29(Suppl. 1), p 84.
F.K. Trefz, et al., “Expanded newborn screening: Long term follow up of 25 patients with organic acidemias and urea cycle disorders”, JOURNAL OF INHERITED METABOLIC DISEASE, vol. 29, 2006, pp. 84.
Trefz, F.K., Töpel, T., Scheible, D., Frauendienst-Egger, G., Hofestädt, R.: Expanded newborn screening: Long term follow up of 25 patients with organic acidemias and urea cycle disorders. JOURNAL OF INHERITED METABOLIC DISEASE. 29, 84 (2006).
Trefz, F. K., Töpel, Thoralf, Scheible, D., Frauendienst-Egger, G., and Hofestädt, Ralf. “Expanded newborn screening: Long term follow up of 25 patients with organic acidemias and urea cycle disorders”. JOURNAL OF INHERITED METABOLIC DISEASE 29.Suppl. 1 (2006): 84.

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