Concepedia

B Wittwer

BW

6

Publications

865

Citations

6

H-Index

1995

Active since

Affiliations

University of Münster(Current)

Ludwig-Maximilians-Universität München

Universitäts-Augenklinik Bonn

University of Lübeck

B Wittwer is an author at University of Münster specializing in genetics, medicine, and gene expression.

Top concepts

Publications per year

1995–2001

6

Publications

6

A gene (RPGR) with homology to the RCC1 guanine nucleotide exchange factor is mutated in X–linked retinitis pigmentosa (RP3)

A Meindl, Katherine L. Dry, Karin A. Herrmann et al. · Nature Genetics · 1996 · 479 citations

, , +11

Genotypic and Phenotypic Spectrum in Tricho-Rhino-Phalangeal Syndrome Types I and III

H.‐J. Lüdecke, Jörg Schaper, Peter Meinecke et al. · The American Journal of Human Genetics · 2001 · 234 citations · Full text

, , +4

Opitz G/BBB Syndrome in Xp22: Mutations in the MID1 Gene Cluster in the Carboxy-Terminal Domain

Karin Gaudenz, Erich Roessler, Nandita Quaderi et al. · The American Journal of Human Genetics · 1998 · 69 citations · Full text

, , +10

A gene (SRPX) encoding a sushi-repeat-containing protein is deleted in patients with X-linked retinitis pigmentosa

Alfons Meindl, Maria Raquel Santos Carvalho, Klaus M. Herrmann et al. · Human Molecular Genetics · 1995 · 57 citations

Clinical presentation and mutation identification in the NBS1 gene in a boy with Nijmegen breakage syndrome

Saskia Kleier, Martin Herrmann, B Wittwer et al. · Clinical Genetics · 2000 · 14 citations

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