G. Hauptmann

Statement on the Nomenclature of Human C4 Allotypes

G. Mauff, Chester A. Alper, Z Awdeh et al. · Immunobiology · 1983 · 227 citations

Human C4 Allotypes, Allelic Variant, Haplotype Determination +6

H deficiency in two brothers with atypical dense intramembranous deposit disease

Micheline Lévy, Lise Halbwachs‐Mecarelli, Marie-Claire Gübler et al. · Kidney International · 1986 · 168 citations · Full text

Mendelian Disorder, Inherited Metabolic Disease, Hematology +4

Allelic repertoire of the humanMHC class IMICA gene

Nassima Fodil, Laurent Laloux, Valérie Wanner et al. · Immunogenetics · 1996 · 160 citations

Histocompatibility, Immunogenetics, Allelic Repertoire +3

Rearrangements and point mutations of P450c21 genes are distinguished by five restriction endonuclease haplotypes identified by a new probing strategy in 57 families with congenital adrenal hyperplasia.

Yves Morel, Jean André, B. Uring‐Lambert et al. · Journal of Clinical Investigation · 1989 · 137 citations · Full text

P450c21 Genes, Cdna Probes, Genetic Testing +14

Inherited deficiency of the fourth component of human complement.

G. Hauptmann, G Tappeiner, J.A. Schifferli · PubMed · 1988 · 134 citations

Histocompatibility, Genetics, Hla Immunogenetics +17