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

Clinical Chemistry and Laboratory Medicine - Germany
doi 10.1515/cclm.1990.28.6.413
Full Text
Abstract

Available in full text

Date
Authors
Publisher

Walter de Gruyter GmbH

Related search

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

Endocrinologia Japonica
1987English

Dna Hybridization Analysis of 21-Hydroxylase Deficiency

Pediatric Research
Child HealthPediatricsPerinatology
1986English

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

Journal of Medical Genetics
Genetics
1989English

Molecular Pathology of 21-Hydroxylase Deficiency

Pediatric Research
Child HealthPediatricsPerinatology
1993English

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

Internal Medicine
Internal MedicineMedicine
2009English

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

Pediatric Research
Child HealthPediatricsPerinatology
1981English

Location of the Gene for 21-Hydroxylase Deficiency

Pediatric Research
Child HealthPediatricsPerinatology
1979English

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

Clinical Pediatric Endocrinology
Child HealthEndocrinologyPerinatologyPediatricsMetabolismDiabetes
1993English

Genetics and Biochemical Variability of Variants of 21 Hydroxylase Deficiency.

Journal of Medical Genetics
Genetics
1985English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2024 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy