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- Identification of compound heterozygous mutations in <i>AP1B1</i> leading to the newly described recessive keratitis–ichthyosis–deafness (KIDAR) syndrome
- The gene for autosomal dominant hidrotic ectodermal dysplasia (Clouston syndrome) in a large Indian family maps to the 13q11-q12.1 pericentromeric region
- Serum phoenixin-14 and phoenixin-20 concentrations in polycystic ovary syndrome: Associations with anti-Müllerian hormone and diagnostic utility
- Guidelines for the Use of Acitretin in Psoriasis
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- SINDROMA CUSHING PADA KEHAMILAN
- Androgenetic alopecia: Traditional cardiovascular risk factors, metabolic syndrome, and component traits among Nigerian adults
- POLİKİSTİK OVER SENDROMU FENOTİPLERİ VE METABOLİK DİSFONKSİYON İLİŞKİSİ
- Evaluation of hyperandrogenemia and metabolic risk profile in women with postadolescent acne
- The prevalence of metabolic syndrome in male patients of early onset androgenic alopecia compared to age matched controls
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