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Research 91–120 of 1000+
- A Novel Missense Mutation Affecting the Human Hairless Thyroid Receptor Interacting Domain 2 Causes Congenital Atrichia
- Clinical, Biochemical and Molecular Characteristics of Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
- Coats' Plus: A Progressive Familial Syndrome of Bilateral Coats' Disease, Characteristic Cerebral Calcification, Leukoencephalopathy, Slow Pre- and Post-Natal Linear Growth and Defects of Bone Marrow and Integument
- Pachyonychia Congenita-Associated Alopecia. A Microscopic Analysis Using Transverse Section Technique
- A Review on-Types and Treatment of Alopecia
- British Hair and Nail Society
- Human ClinicalPhenotype Associated with FOXN1 Mutations
- <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
- Inherited Hairlessness: A Case Study of Familial Congenital Atrichia
- Clinical report of a Holstein's calf with ichthyosis.
- Hair loss in infancy and childhood
- 农民致富的领路人——记“省青年星火带头人标兵”叶明
- What Work-Up Should Be Done for Patients With Alopecia?
- Congenital triangular alopecia: A close mimicker of alopecia areata
- Congenital Adrenal Hyperplasia
- Hair Loss in Children
- Molecular basis of congenital atrichia in humans and mice.
- Hair loss in children.
- Paint brush hair: a case report
- Management of congenital ichthyoses: European guidelines of care, part two
- Congenital Copper Deficiency: Copper Therapy and Dopamine‐β‐Hydroxylase Activity in the Mottled (Brindled) Mouse
- A Brazilian case of IFAP syndrome with severe congenital ichthyosis and limb malformations caused by a rare variant in MBTPS2
- P142 – 3046: Encephalocraniocutaneous lipomatosis, a rare neurocutaneous disorder: Report of additional three cases
- Psychotrichology: psychosomatic aspects of hair diseases
- Hair loss in infancy and childhood
- Office Diagnosis of Hair Shaft Defects
- Skin Development and Disease: A Molecular Perspective
- Hair transplantation between identical twins
- ODP408 Elevated DHEAS and Acute Hair Loss in an Adult Male with Trichorhinophalangeal Syndrome Type 1: a Case of Male PCOS
- Congenital and Hereditary Skin Diseases