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Publications by L. Kochhan

HLA Class I-, Complement C4- And 21-Hydroxylase Probes in the Genetic Analysis of 21-Hydroxylase Deficiency

Clinical Chemistry and Laboratory Medicine

Clinical Biochemistry

English

Related publications

Analysis of Steroid 21-Hydroxylase Gene in Five Unrelated Japanese Patients With 21-Hydroxylase Deficiency

Endocrinologia Japonica

English

Dna Hybridization Analysis of 21-Hydroxylase Deficiency

Pediatric Research

English

21-Hydroxylase Deficiency Families With HLA Identical Affected and Unaffected Sibs.

Journal of Medical Genetics

English

Molecular Pathology of 21-Hydroxylase Deficiency

Pediatric Research

English

Genetic Analysis of Two Japanese Patients With Non-Classical 21-Hydroxylase Deficiency

Internal Medicine

Internal Medicine

English

HLA and Hormonal Studies in Families of Patients With 21-Hydroxylase Deficiency - Cryptic Patients?

Pediatric Research

English

Location of the Gene for 21-Hydroxylase Deficiency

Pediatric Research

English

Genetic Analysis of Classical 21-Hydroxylase Deficiency Using Polymerase Chain Reaction and Allele-Specific Oligonucleotide Hybridization

Clinical Pediatric Endocrinology

English

Genetics and Biochemical Variability of Variants of 21 Hydroxylase Deficiency.

Journal of Medical Genetics

English