Search
forResearch 10 of 1000+
- Keratoma Hereditaria Mutilans (Vohwinkel's Disease) with Congenital Alopecia Universalis (Atrichia Congenita)
- A rare cause of irrevocable childhood alopecia feigning alopecia universalis: Atrichia congenita with papular lesions
- PA31 Congenital alopecia areata: a systematic review
- Atrichia congenita with papular lesions: A rare cause of pediatric alopecia
- Alopecia universalis and Kallman’s Syndrome
- Clinical and Molecular Diagnostic Criteria of Congenital Atrichia with Papular Lesions11This paper originally appeared in issue 117:1662–1665, 2001. Following publication the authors indicated that important corrections at page proof were not taken in. To ensure that the paper is published as intended, the editors have decided to reproduce the contents in full.
- A Novel Missense Mutation Affecting the Human Hairless Thyroid Receptor Interacting Domain 2 Causes Congenital Atrichia
- Commonly associated disorders with complete scalp alopecia in early childhood: A review
- FOXN1 deficient nude severe combined immunodeficiency
- Reply
Learn
— no results
Try a deeper search in learn →Community
— no results
Try a deeper search in community →