W. Wolz

发表

New mutations in the ataxia telangiectasia gene

H. Hoehn, D. Schindler, A. Baumer, 1996, Human Genetics.

Identification of novel mutations in the ryanodine-receptor gene (RYR1) in malignant hyperthermia: genotype-phenotype correlation.

G. Comi, M. Lehane, A. Urwyler, 1998, American journal of human genetics.

Novel mutations at a CpG dinucleotide in the ryanodine receptor in malignant hyperthermia

G. Comi, A. Urwyler, J. Lunardi, 1998, Human mutation.

Homozygosity mapping of a second gene locus for hereditary combined deficiency of vitamin K-dependent clotting factors to the centromeric region of chromosome 16.

J. Oldenburg, A. Fregin, S. Rost, 2002, Blood.

The human gene for alkaptonuria (AKU) maps to chromosome 3q.

J. Guénet, W. Kress, X. Montagutelli, 1994, Genomics.

A genome wide search for susceptibility loci in three European malignant hyperthermia pedigrees.

C. van Broeckhoven, A. Reis, T. Deufel, 1997, Human molecular genetics.

Sorsby's fundus dystrophy is genetically linked to chromosome 22q13–qter

E. Ives, W. Wolz, B. Weber, 1994, Nature Genetics.

Homozygosity Mapping of a Second Gene Locus for Hereditary Combined Deficiency of Vitamin K-Dependent Clotting Factors (FMFD) to Chromosome 16

J. Oldenburg, A. Fregin, S. Rost, 2004 .

Congenital Deficiency of Vitamin K Dependent Coagulation Factors in Two Families Presents as a Genetic Defect of the Vitamin K-Epoxide-Reductase-Complex

L. Schurgers, J. Oldenburg, A. Fregin, 2000, Thrombosis and Haemostasis.

Genomic sequence and organization of the human gene for cytochrome c oxidase subunit (COX7A1) VIIa-M.

W. Kress, C. Mueller, W. Wolz, 1997, Genomics.

First Case of Compound Heterozygosity in the Gamma- Glutamyl Carboxylase Gene Causing Combined Deficiency of all Vitamin K-Dependent Blood Coagulation Factors

J. Oldenburg, A. Fregin, S. Rost, 2004 .