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Research 931–960 of 1000+
- Sjogren-Larsson syndrome
- 4 Vitamin D resistance
- Analysis of the relationship between the mutation site of the SLC39A4 gene and acrodermatitis enteropathica by reporting a rare Chinese twin: a case report and review of the literature
- Papillon–Lefèvre Syndrome: A Rare Case Report of Two Brothers and Review of the Literature
- A Heritable Keratinization Defect of the Superficial Epidermis in Norfolk Terriers
- Siberian cats help in solving part of the mystery surrounding golden cats
- Topical minoxidil improves congenital hypotrichosis caused by <i>LIPH</i> mutations
- The medusa head: Dermoscopic diagnosis of woolly hair syndrome
- Alopezien und Hypotrichosen im Kindesalter
- Forme létale de syndrome de Netherton au sein d’une famille multiplex consanguine
- Congenital atrichia with papular lesions
- Monilethrix
- A Homozygous Missense Variant in K25 Underlying Overlapping Phenotype with Woolly Hair and Dental Anomalies
- Congenital Hypotrichosis in Japanese White Strain (JW-NIBS) Rabbits.
- Mutation des menschlichen hairless -Gens bei Atrichia universalis
- Ugreelig hår
- A Newborn With Hair Loss
- Woolly Antics between the Sheaths
- Reply
- The systemic wrinkled skin phenotype involves aberrant expression and variation of genes related to the oxidative stress and extracellular matrix in Xiang pigs
- Neonatal ichthyosis-sclerosing cholangitis syndrome caused by a novel CLDN1 mutation: a case report and literature review
- Unusual Dermatologic Findings in an Extremely Low Birthweight Infant: The Genetic Diagnosis
- Woolly hair generalizado: caso clínico e revisão da literatura
- Differential expression of keratin and keratin associated proteins are linked with hair loss condition in spontaneously mutated inbred mice
- Reviewer #3 (Public Review): CaBP1 and 2 enable sustained CaV1.3 calcium currents and synaptic transmission in inner hair cells
- Syndromic or non-syndromic congenital ichthyosis? A case report of two brothers with ichthyosis but microphthalmia and blindness in only one brother
- Congenital Atrichia: A Case Report
- Molecular Basis of Hereditary Hair Diseases
- Inherited Hairlessness: A Case Study of Familial Congenital Atrichia
- Uncombable hair syndrome due to maternal uniparental disomy of chromosome 1