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Research 91–120 of 1000+
- 7745 Hirsutism in young girls, Beyond PCOS
- Multiple congenital smooth muscle hamartoma: A case report
- Hereditary, Congenital, and Acquired Alopecias
- Netherton's syndrome: A syndrome of elevated IgE and characteristic skin and hair findings
- Recommendations for treatment of nonclassic congenital adrenal hyperplasia (NCCAH): An update
- Nonclassic Congenital Adrenal Hyperplasia
- A novel missense mutation (C622G) in the zinc‐finger domain of the human hairless gene associated with congenital atrichia with papular lesions
- Congenital alopecia areata
- Generalized Congenital Hypotrichosis in a Female Rottweiler
- Congenital triangular alopecia
- Novel small‐insertion mutation in the <i>LIPH</i> gene in a patient with autosomal recessive woolly hair/hypotrichosis
- Familial congenital generalized hypertrichosis
- Berardinelli–Seip syndrome
- Clinical, Biochemical and Molecular Characteristics of Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
- Woolly hair generalizado: caso clínico e revisão da literatura
- Syndromic or non-syndromic congenital ichthyosis? A case report of two brothers with ichthyosis but microphthalmia and blindness in only one brother
- A solitary triangular alopecia
- Inherited Hairlessness: A Case Study of Familial Congenital Atrichia
- T Cell Immunodeficiency, Congenital Alopecia, and Nail Dystrophy
- Localized Acquired Alopecia over the Mental Area of Chin
- A case of temporal triangular alopecia
- Fixed focal alopecia for 20 years
- The hairless (hr) gene is involved in the congential hypotrichosis of Valle del Belice sheep
- Congenital adrenal hyperplasia
- Molecular basis of congenital atrichia in humans and mice.
- Epicardial Fat Thickness in Children with Classic Congenital Adrenal Hyperplasia
- Novel Systematics of Nomenclature and Classification of Female Functional Androgenization (Including Polycystic Ovary Syndrome and Non-Classic Congenital Adrenal Hyperplasia)
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- Congenital atrichia associated with situs inversus and mesocardia
- Congenital localized basaloid follicular hamartoma: a case report and review of the literature