B. Wittwer

发表

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

A. Ciccodicola, M. D'urso, T. Meitinger, 1996, Nature Genetics.

Opitz G/BBB syndrome in Xp22: mutations in the MID1 gene cluster in the carboxy-terminal domain.

A. Ballabio, J. Opitz, B. Wittwer, 1998, American journal of human genetics.

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

M. Herrmann, B. Wittwer, A. Reis, 2000, Clinical genetics.

X-linked retinitis pigmentosa: RPGR mutations in most families with definite X linkage and clustering of mutations in a short sequence stretch of exon ORF15.

T. Meitinger, B. Lorenz, A. Meindl, 2003, Investigative ophthalmology & visual science.

Genotypic and phenotypic spectrum in tricho-rhino-phalangeal syndrome types I and III.

N. Niikawa, K. Devriendt, R. Hennekam, 2001, American journal of human genetics.

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

T. Meitinger, B. Lorenz, A. Meindl, 1995, Human molecular genetics.

Submicroscopic deletion in 14q32.3 through a de novo tandem translocation between 14q and 21p.

B. Wittwer, J. Horst, D. Meschede, 1998, American journal of medical genetics.

New X-linked mental retardation syndrome with the gene mapped tentatively in Xp22.3.

B. Wittwer, J. Leutelt, A. Gal, 1996, American journal of medical genetics.

Yunis‐Varon syndrome: the first case of German origin

B. Wittwer, J. Horst, G. Jorch, 1996, Clinical dysmorphology.

Further localization of X-linked hydrocephalus in the chromosomal region Xq28.

S. Warren, C. Broeckhoven, B. Wittwer, 1992, American journal of human genetics.

Erratum: Opiz G/BBB syndrome in Xp22: Mutations in the MID1 gene cluster in the carboxy-terminal domain (American Journal of Human Genetics (September 1998) 63 (703-710))

A. Ballabio, B. Wittwer, M. Muenke, 1998 .