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Research 31–60 of 1000+
- Congenital atrichia and hypotrichosis
- Autosomal recessive hypotrichosis simplex with woolly hair: a report of a new family
- Molecular Basis of Hereditary Hair Diseases
- Congenital and Hereditary Skin Diseases
- Congenital and Hereditary Skin Diseases
- Clinical and molecular genetic studies in hereditary hair loss
- Genetics of Structural Hair Disorders
- Inherited Disorders of the Hair
- Hair: more than just an appendage
- Editors' Picks
- News in brief
- Coat Problems
- Polarized microscopy in genetic hair disorders: case series
- Mutations in SNRPE, which Encodes a Core Protein of the Spliceosome, Cause Autosomal-Dominant Hypotrichosis Simplex
- Poly(rC) binding protein 2 acts as a negative regulator of IRES-mediated translation of Hr mRNA
- Recalcitrant Female Pattern Hair Loss Like Alopecia Unveils Unexpected Rare Entity
- Two females with hair loss
- Odd-Looking Hair and Progressive Alopecia in Mother and Son
- Monilethrix: Beaded hair and hypotrichosis in a child
- BG01 Confirming small nuclear ribonucleoprotein polypeptide E as a cause of nonsyndromic hypotrichosis
- Pathology in Practice
- Critical Evaluation of Concept of Genetics in Ayurveda WSR to Eight Undesired Body Types (Ashta Nindit)
- Description of clinical aspects and microscopy of the hair shaft of a carrier of familial monilethrix
- Biology and Genetics of Hair
- Autosomal recessive woolly hair/hypotrichosis with homozygous mutation in the <i>LIPH</i> gene: a case report
- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle
- Moniletrix of the scalp from almost normal aspect to total alopecia: variable intrafamilial expressiveness
- Current Genetics in Hair Diseases
- Ectodermal Dysplasia: Variable Expressions
- A rare hair loss in children: Monilethrix