Search
for
Sort by
Research 361–390 of 1000+
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- A new type of pachyonychia congenita.
- A new case of Ambras syndrome associated with a paracentric inversion (8) (q12; q22)
- Cholesterol homeostasis: Links to hair follicle biology and hair disorders
- 农民致富的领路人——记“省青年星火带头人标兵”叶明
- Coat Problems
- Office Diagnosis of Hair Shaft Defects
- Metabolic and pathologic profiles of human LSS deficiency recapitulated in mice
- A frameshift insertion in SGK3 leads to recessive hairlessness in Scottish Deerhounds: a candidate gene for human alopecia conditions
- Genetics of Alopecia
- A clinician's approach to canine alopecia
- Hair Shaft Abnormalities. Pili Bifurcati: A Scanning Electron Microscopy Analysis
- ACP Broadsheet 131: March 1992. Hirsute women: should they be investigated?
- Hirsutism and Virilization in the Female
- The hair in childhood and old age
- ‘Black dots’ seen under trichoscopy are not specific for alopecia areata
- Woolly hair generalizado: caso clínico e revisão da literatura
- Clinical and molecular genetic studies in hereditary hair loss
- Index
- Hair Disorders
- Case Report: Compound heterozygous variants in LSS and TSPEAR genes causing hypotrichosis type 14 complicated with ectodermal dysplasia type 14
- Congenital hair loss disorders: Rare, but not too rare
- Two Cases of Hypertrichosis Cubiti
- Molecular basis of hypotrichosis with juvenile macular dystrophy in two siblings
- Recalcitrant Female Pattern Hair Loss Like Alopecia Unveils Unexpected Rare Entity
- Distinct genotype-phenotype patterns in non-syndromic hereditary hypotrichosis: a multicenter Chinese cohort
- Pathogenesis and causes of hirsutism
- Disorders of hair growth : diagnosis and treatment
- Becker's Nevus Syndrome
- Disorders of the Hair and Nails