F. Lorenzen

发表

Genotyping steroid 21-hydroxylase deficiency: hormonal reference data.

B. Kohn, M. New, B. Dupont, 1983, The Journal of clinical endocrinology and metabolism.

Genetic and hormonal characterization of cryptic 21-hydroxylase deficiency.

B. Kohn, C. Scaroni, L. Tatò, 1981, The Journal of clinical endocrinology and metabolism.

Improved test to identify heterozygotes for congenital adrenal hyperplasia without index case examination

W. Sippell, M. Peter, E. Westphal, 1990, The Lancet.

Treatment of children with central precocious puberty by a slow-release gonadotropin-releasing hormone agonist

R. Odink, W. Sippell, S. Drop, 1990, European Journal of Pediatrics.

HLA linkage and B14, DR1, BfS haplotype association with the genes for late onset and cryptic 21-hydroxylase deficiency.

B. Kohn, M. New, B. Dupont, 1981, American journal of human genetics.

"Acquired" adrenal hyperplasia with 21-hydroxylase deficiency is not the same genetic disorders as congenital adrenal hyperplasia.

M. New, B. Dupont, S. Pang, 1979, The Journal of clinical endocrinology and metabolism.

HLA‐A,B,C,DR typing and 17‐OHP determination for second trimester prenatal diagnosis of 21‐hydroxylase deficient CAH

E. Passarge, W. Sippell, F. Bidlingmaier, 1988, Prenatal diagnosis.

DETECTION OF HETEROZYGOTE OF 21-HYDROXYLASE DEFICIENCY

M. New, B. Dupont, M. Pollack, 1980, The Lancet.

Studies of the C-21 and C-19 steroids and HLA genotyping in siblings and parents of patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

M. New, B. Dupont, S. Pang, 1980, The Journal of clinical endocrinology and metabolism.

Hormonal Phenotype and HLA-Genotype in Families of Patients with Congenital Adrenal Hyperplasia (21-Hydroxylase Deficiency)

M. New, B. Dupont, M. Pollack, 1979, Pediatric Research.

“Acquired” Adrenal Hyperplasia with 21-Hydroxylase Deficiency is Not the Same Genetic Disorder as Congenital Adrenal Hyperplasia

M. New, B. Dupont, S. Pang, 1979 .

Cryptic 21-hydroxylase deficiency in families of patients with classical congenital adrenal hyperplasia.

B. Kohn, C. Scaroni, M. New, 1980, The Journal of clinical endocrinology and metabolism.

Late-onset steroid 21-hydroxylase deficiency: a variant of classical congenital adrenal hyperplasia.

B. Kohn, M. New, B. Dupont, 1982, The Journal of clinical endocrinology and metabolism.

Targeted Resequencing of Putative Growth-Related Genes Using Whole Exome Sequencing in Patients with Severe Primary IGF-I Deficiency

H. Reutter, M. Ludwig, A. Hilger, 2017, Hormone Research in Paediatrics.

Late onset 21-hydroxylase deficiency and HLA in the Ashkenazi population: a new allele at the 21-hydroxylase locus.

Z. Laron, M. New, B. Dupont, 1980, Human immunology.

Hormonal studies in obligate heterozygotes and siblings of patients with 11 beta-hydroxylase deficiency congenital adrenal hyperplasia.

M. Genel, M. New, B. Dupont, 1980, The Journal of clinical endocrinology and metabolism.