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Research 121–150 of 1000+
- 882 Syndactyly type III and hypotrichosis in oculodentodigital syndrome with GJA1 mutation
- The eyelash comes to the fore
- Metreleptin Treatment in a Boy with Congenital Generalized Lipodystrophy due to Homozygous c.465_468delGACT (p.T156Rfs*8) Mutation in the BSCL2 Gene: Results From the First-year
- 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.
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- A Novel Missense Mutation Affecting the Human Hairless Thyroid Receptor Interacting Domain 2 Causes Congenital Atrichia
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Four hypotrichosis families with mutations in the gene <i>LSS</i> presenting with and without neurodevelopmental phenotypes
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Familial Pure Hair–Nail Ectodermal Dysplasia in Yemen: A Father–Son Case Report with Clinical Correlation
- Role of trichoscopy in diagnosis of different hair and scalp disorders in pediatrics
- Secondary cicatricial and other permanent alopecias
- Female Adolescent Hair Disorders
- Hormonal profile and androgen receptor study in prepubertal girls with hypertrichosis
- Acquired Generalized Hypertrichosis Due to Diazoxide
- Multiple congenital smooth muscle hamartoma: A case report
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- A Practical Approach to the Diagnosis and Management of Hair Loss in Children and Adolescents
- Hair Loss in Children
- Clinical relevance of hair microscopy in alopecia
- Congenital atrichia associated with situs inversus and mesocardia
- Marie-unna hereditary hypotrichosis
- Congenital Trichomegaly of the Eyelashes
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- Congenital atrichia associated with nevus flammeus: A rare association
- An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis
- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers
- A position effect on TRPS1 is associated with Ambras syndrome in humans and the Koala phenotype in mice
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex
- Hairless is a nuclear receptor corepressor essential for skin function