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Research 631–660 of 1000+
- A newborn presenting with congenital blistering
- Hereditary vitamin D rickets: a case series in a family
- Werner′s syndrome
- Monilethrix, a rare inherited hair shaft disorder in siblings
- Delayed-onset pachyonychia congenita caused by a novel mutation in the V2 domain of keratin 6b
- Case Report: A Chinese Family of Woodhouse-Sakati Syndrome With Diabetes Mellitus, With a Novel Biallelic Deletion Mutation of the DCAF17 Gene
- Hutchinson-Gilford progeria syndrome: Report of 2 cases and a novel LMNA mutation of HGPS in China
- PLACK syndrome associated with alopecia areata and a novel homozygous base pair insertion in exon 18 of CAST gene
- 199 Impairment of notch 1 signaling is a common defect in lesions from patients with hidradenitis suppurativa
- A 40-Year-Old Woman With Facial Papules and Flank Pain
- ADULT (acro–dermato–ungual–lacrimal–tooth) syndrome: A case report from India
- Rickets with Alopecia Signals Vitamin D Dependent Rickets Type II
- Björnstad Syndrome With Late‐Onset Alopecia Mimicking Androgenetic Alopecia: Histopathological and Genetic Findings
- Androgenic alopecia and differential diagnoses of alopecia
- Clinical cases of Darier-White follicular dyskeratosis
- Moniletrix of the scalp from almost normal aspect to total alopecia: variable intrafamilial expressiveness
- Hair: more than just an appendage
- Loose anagen syndrome in one identical twin girl.
- Ichthyosis Follicularis with Alopecia and Photophobia Syndrome (IFAP): A Case Report and Review of the Literature
- Loose Anagen Syndrome
- Congenital and Hereditary Skin Diseases
- Genetics and Pathophysiology of Congenital Adrenal Hyperplasia
- Bamboo Hair Syndrome or Netherton Syndrome - A Case Report
- Hair Anomalies in a 6-Year-Old Girl
- Emergence of hereditary hyperplastic gingivitis in Newfoundland and Labrador, Canada: an exploration into the molecular aetiology at both the gene and genome levels
- Hair dysplasias
- The Case | Bilateral kidney tumors and lung cysts
- Novel frameshift mutation in TRPS1 in a ukrainian patient with trichorhinophalangeal syndrome type I
- Management of pregnancy in a carrier of the Donohue mutation
- Targeting integrin pathways: mechanisms and advances in therapy