Darstellung, Methode und Struktur : Untersuchungen zur Einheit der systematischen Philosophie G. W. F. Hegels /

Por Puntel, Lorenz B.
Publicado em 1981

Causes of blindness at the “Wiyata Guna” School for the Blind, Indonesia

Por Sitorus, R, Preising, M, Lorenz, B
Publicado em 2003

CYP1B1 gene analysis in primary congenital glaucoma in Indonesian and European patients

Por Sitorus, R, Ardjo, S, Lorenz, B, Preising, M
Publicado em 2003

First molecular evidence for a de novo mutation in RS1 (XLRS1) associated with X linked juvenile retinoschisis

Por GEHRIG, A., WEBER, B., LORENZ, B., ANDRASSI, M.
Publicado em 1999

Recurrent 3-bp deletion at codon 255/256 of the rhodopsin gene in a German pedigree with autosomal dominant retinitis pigmentosa.

Por Artlich, A, Horn, M, Lorenz, B, Bhattacharga, S, Gal, A
Publicado em 1992

Deletion in the OA1 gene in a family with congenital X linked nystagmus

Por Preising, M., de Laak, J.-P. O., Lorenz, B.
Publicado em 2001

Heterozygous P250L mutation of fibroblast growth factor receptor 3 in a case of isolated craniosynostosis

Por Schindler, S, Friedrich, M, Wagener, H, Lorenz, B, Preising, M
Publicado em 2002

Unexpected Genetic Cause in Two Female Siblings with High Myopia and Reduced Visual Acuity

Por Preising, M. N., Friedburg, C., Bowl, W., Lorenz, B.
Publicado no Biomed Res Int (2018)

Constitutional RB1-gene mutations in patients with isolated unilateral retinoblastoma.

Por Lohmann, D R, Gerick, M, Brandt, B, Oelschläger, U, Lorenz, B, Passarge, E, Horsthemke, B
Publicado em 1997

Features of mtDNA mutation patterns in European pedigrees and sporadic cases with Leber hereditary optic neuropathy.

Por Obermaier-Kusser, B., Lorenz, B., Schubring, S., Paprotta, A., Zerres, K., Meitinger, T., Meire, F., Cochaux, P., Blankenagel, A., Kommerell, G.
Publicado em 1994

Toward genome editing in X-linked RP—development of a mouse model with specific treatment relevant features

Por Schlegel, J., Hoffmann, J., Röll, D., Müller, B., Günther, S., Zhang, W., Janise, A., Vössing, C., Fühler, B, Neidhardt, J., Khanna, H., Lorenz, B., Stieger, K.
Publicado no Transl Res (2019)

Nanodomain induced anomalous magnetic and electronic transport properties of LaBaCo(2)O(5.5+δ) highly epitaxial thin films

Por Ruiz-Zepeda, F., Ma, C., Bahena Uribe, D., Cantu-Valle, J., Wang, H., Xu, Xing, Yacaman, M. J., Chen, C., Lorenz, B., Jacobson, A. J., Chu, P. C. W., Ponce, A.
Publicado em 2014