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Publications by V Pucholt

Location of the Gene for 21-Hydroxylase Deficiency

Pediatric Research
Child HealthPediatricsPerinatology
1979English

Related publications

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

Endocrinologia Japonica
1987English

Molecular Pathology of 21-Hydroxylase Deficiency

Pediatric Research
Child HealthPediatricsPerinatology
1993English

Dna Hybridization Analysis of 21-Hydroxylase Deficiency

Pediatric Research
Child HealthPediatricsPerinatology
1986English

Use of Nonradioactive Labeling to Detect Large Gene Rearrangements in 21-Hydroxylase Deficiency

Revista do Hospital das Clínicas
2004English

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

Clinical Chemistry and Laboratory Medicine
BiochemistryMedicineClinical Biochemistry
1990English

Genetics and Biochemical Variability of Variants of 21 Hydroxylase Deficiency.

Journal of Medical Genetics
Genetics
1985English

Classic Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency

2020English

Deletion of the 21-Hydroxylase Gene in Congenital Adrenal Hyperplasia

Pediatric Research
Child HealthPediatricsPerinatology
1986English

Identification of a Novel Compound Heterozygous Mutation of the CYP21A2 Gene Causing 21‑hydroxylase Deficiency in a Chinese Pedigree

Molecular Medicine Reports
OncologyGeneticsMolecular BiologyBiochemistryCancer ResearchMolecular Medicine
2018English

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