E. Fleischnick

发表

EXTENDED MHC HAPLOTYPES IN 21-HYDROXYLASE-DEFICIENCY CONGENITAL ADRENAL HYPERPLASIA: SHARED GENOTYPES IN UNRELATED PATIENTS

J. Granados, E. Yunis, S. Alosco, 1983, The Lancet.

Extended major histocompatibility complex haplotypes in patients with gluten-sensitive enteropathy.

E. Yunis, C. Alper, Z. Awdeh, 1987, The Journal of clinical investigation.

Extended major histocompatibility complex haplotypes in patients with multiple sclerosis

H. Weiner, S. Hauser, E. Yunis, 1989, Neurology.

Progressive Autoimmune Beta Cell Insufficiency: Occurrence in the Absence of High-Risk HLA Alleles DR3, DR4

G. Eisenbarth, O. Ganda, S. Brink, 1985, Diabetes Care.

The distribution of human C4 DNA variants in relation to major histocompatibility complex alleles and extended haplotypes.

L. Truedsson, P. Schneider, A. Whitehead, 1988, Human immunology.

DNA polymorphism of the C4 genes. A new marker for analysis of the major histocompatibility complex.

H. Colten, A. Whitehead, D. Woods, 1984, The New England journal of medicine.

Pre-Type 1 (insulin-dependent) diabetes: common endocrinological course despite immunological and immunogenetic heterogeneity

O. Ganda, S. Brink, R. Jackson, 1984, Diabetologia.

Tapetoretinal degeneration associated with multisystem abnormalities. A case report.

T. Hirose, O. Katsumi, F. Shapiro, 1986, Ophthalmic paediatrics and genetics.

Complement genes of the human major histocompatibility complex: implications for linkage disequilibrium and disease associations

E. Yunis, C. Alper, Z. Awdeh, 1984 .

The autosomal dominant form of “pure” familial spastic paraplegia

M. Spence, M. Marazita, E. Kolodny, 1987, Neurology.

Detection of late-onset 21-hydroxylase deficiency congenital adrenal hyperplasia in adolescents.

S. Emans, M. Mansfield, E. Grace, 1983, Pediatrics.