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Research 721–750 of 1000+
- A case of monilethrix caused by novel compound heterozygous mutations in the desmoglein 4 (DSG4) gene
- Cellular and Metabolic Basis for the Ichthyotic Phenotype in NIPAL4 (Ichthyin)–Deficient Canines
- New familial association between ocular coloboma and loose anagen syndrome
- Molecular Genetics of Keratinization Disorders – What’s New About Ichthyosis
- A novel missense mutation in the mouse hairless gene causes irreversible hair loss: Genetic and molecular analyses of Hrm1Enu
- 4 Vitamin D resistance
- Papillon–Lefèvre Syndrome: A Rare Case Report of Two Brothers and Review of the Literature
- CDH3 gene related hypotrichosis and juvenile macular dystrophy – A case with a novel mutation
- Congenital atrichia with papular lesions
- Topical minoxidil improves congenital hypotrichosis caused by <i>LIPH</i> mutations
- Alopezien und Hypotrichosen im Kindesalter
- Congenital atrichia with papular lesions
- Monilethrix
- Hypotrichosis with Juvenile Macular Dystrophy in Saudi Arabia: A Case Report
- Mutation des menschlichen hairless -Gens bei Atrichia universalis
- Congenital Hypotrichosis in Japanese White Strain (JW-NIBS) Rabbits.
- A Newborn With Hair Loss
- Reviewer #3 (Public Review): CaBP1 and 2 enable sustained CaV1.3 calcium currents and synaptic transmission in inner hair cells
- Congenital Atrichia: A Case Report
- INDENTIFICATION OF GENES INVOLVED IN INHERITED ECTODERMAL DYSPLASIAS
- Lanceolate hair-J (lahJ): a mouse model for human hair disorders [In Process Citation]
- Neonatal ichthyosis-sclerosing cholangitis syndrome caused by a novel CLDN1 mutation: a case report and literature review
- Differential expression of keratin and keratin associated proteins are linked with hair loss condition in spontaneously mutated inbred mice
- Syndromic or non-syndromic congenital ichthyosis? A case report of two brothers with ichthyosis but microphthalmia and blindness in only one brother
- Inherited Hairlessness: A Case Study of Familial Congenital Atrichia
- Evaluation of hair structural abnormalities in children with different neurological diseases
- A rare cause of irrevocable childhood alopecia feigning alopecia universalis: Atrichia congenita with papular lesions
- Clinical report of a Holstein's calf with ichthyosis.
- 190 Deficiency of the Human Cysteine Protease Inhibitor Cystatin M/E Causes Hypotrichosis and Dry Skin
- Disorders of Keratinization