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Research 661–690 of 1000+
- Dermatopathia pigmentosa reticularis: A report of a case with delayed onset alopecia and onychodystrophy
- Congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency epidemiology, etiopathogenesis, clinical presentation, treatment – a systematic review
- Vitamin D dependent rickets type 2: a case-based review of patient with alopecia and rickets
- Trichothiodystrophy in a child with occult learning disorder
- Congenital Adrenal Hyperplasia
- Congenital Adrenal Hyperplasia
- Vesicle Formation and Follicular Root Sheath Separation in Mice Homozygous for Deleterious Alleles at the Balding (bal) Locus
- Vitamin D‐dependent rickets Type II with alopecia: two case reports and review of the literature
- Nonclassic congenital adrenal hyperplasia
- Cutaneous Ultrastructural Features of the Flaky Skin (<i>fsn</i>) Mouse Mutation
- <i>De novo</i> mutations in monilethrix
- Homozygous Deletion in CDH3 and Hypotrichosis With Juvenile Macular Dystrophy
- <i>TRPS1</i> mutation associated with trichorhinophalangeal syndrome type 1 with 15 supernumerary teeth, hypoplastic mandibular condyles with slender condylar necks and unique hair morphology
- Acrodermatitis enteropathica: Case report analyses of zinc metabolism electron microscopic examination and immune function
- Dermatopathia Pigmentosa Reticularis with Salzmann’s nodular degeneration of cornea: A rare association
- Type II Vitamin D Dependent Rickets: A Case Report
- Hypotrichosis with juvenile macular dystrophy
- Telogen hair loss and androgenetic‐like alopecia in GAPO syndrome
- Inherited Acrodermatitis Enteropathica
- Adli Uygulamalarda Yeni Nesil Dizileme Teknolojilerinin Yeri ve Önemi
- Atrichia with Papular Lesions: Dermoscopy to the Rescue
- P-19 A case of Birt Hogg Dube syndrome presented with parathyroid carcinoma
- Case Report: Bi-allelic missense variant in the desmocollin 3 gene causes hypotrichosis and recurrent skin vesicles
- Papular atrichia
- Photosensitive Trichothiodystrophy with Complex Cerebral Abnormalities
- Acrodermatitis enteropathica: Case report analyses of zinc metabolism electron microscopic examination and immune function
- Improving human forensics through advances in genetics, genomics and molecular biology
- A missense mutation in the type II hair keratin hHb3 is associated with monilethrix
- <i>C2orf37</i> mutational spectrum in Woodhouse–Sakati syndrome patients
- Congenital adrenal hyperplasia