P. Wieacker

Nuclear Lamin-A Scales with Tissue Stiffness and Enhances Matrix-Directed Differentiation

Chromosome Abnormalities and Genetic Counseling

Intersexuality and Gender Identity Differentiation

The retinol acid receptor B gene is hypermethylated in patients with familial partial lipodystrophy

Laminopathies: Multiple disorders arising from defects in nuclear architecture

Prevalence of Muscular Dystrophies: A Systematic Literature Review

Diagnosis and Treatment of Polycystic Ovary Syndrome: An Endocrine Society Clinical Practice Guideline

The Androgen Excess and PCOS Society criteria for the polycystic ovary syndrome: the complete task force report

Rothmund-Thomson syndrome: Review of the world literature

Consensus Statement on Management of Intersex Disorders

Health Supervision for Children With Down Syndrome

The Diagnosis of Polycystic Ovary Syndrome during Adolescence

Gender Change in 46,XY Persons with 5α-Reductase-2 Deficiency and 17β-Hydroxysteroid Dehydrogenase-3 Deficiency

ICRP PUBLICATION 118: ICRP Statement on Tissue Reactions and Early and Late Effects of Radiation in Normal Tissues and Organs — Threshold Doses for Tissue Reactions in a Radiation Protection Context

Endocrine Treatment of Gender-Dysphoric/Gender-Incongruent Persons: An Endocrine Society* Clinical Practice Guideline

Insulin Resistance and the Polycystic Ovary Syndrome Revisited: An Update on Mechanisms and Implications

Role of Hormones in Pilosebaceous Unit Development

p.S143F mutation in lamin A/C: A new phenotype combining myopathy and progeria

Intrachromosomal triplication 12p11.22–p12.3 and gonadal mosaicism of partial tetrasomy 12p^,**

Ein Fall von pseudovaginaler, perineoskrotaler Hypospadie mit 5α-Reduktase-Defizienz

Influence of steroid hormones on 5α-reductase activity in female and male genital skin fibroblasts in culture

Gonadotropinresistenz beim Rothmund-Thomson-Syndrom