S. Mayer

发表

OPA1 mutations in patients with autosomal dominant optic atrophy and evidence for semi-dominant inheritance.

E. Zrenner, B. Jurklies, B. Wissinger, 2001, Human molecular genetics.

Restriction fragment length polymorphism of DP genes defines three new DP alleles

Y. Mitsuishi, S. Mayer, M. Tongio, 2004, Immunogenetics.

HLA and down syndrome (DS): Parents at the origin of the nondisjunction share no more HLA‐A and ‐B antigens with their DS child than controls

C. Stoll, D. Rao, S. Mayer, 1988, Genetic epidemiology.

INFLUENCE OF THE MAJOR HISTOCOMPATIBILITY COMPLEX IN THE PIG (SLA) ON SERUM HAEMOLYTIC COMPLEMENT LEVELS

S. Mayer, M. Vaiman, G. Hauptmann, 1978, Journal of immunogenetics.

OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28

S. Bhattacharya, M. Votruba, A. Moore, 2000, Nature Genetics.

CNGA3 mutations in hereditary cone photoreceptor disorders.

S. Jacobson, R. Salati, L. Sharpe, 2001, American journal of human genetics.

ASSOCIATION OF THE C2‐DEFICIENCY GENE (C2*QO) WITH THE C4A*4, C4B*2 GENES

R. Fauchet, A. Sobel, S. Mayer, 1982, Journal of immunogenetics.

C4 Haplotypes with Duplicated C4A or C4B: Frequency and Associations with Bf, C2, and HLA-A, B, C, DR Alleles with Special Reference to the Duplication C4B1,2

S. Mayer, B. Uring-Lambert, G. Hauptmann, 1984 .