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Research 631–660 of 1000+
- Baker′s dozen on the scalp: An interesting case of multiple trichilemmal cyst
- A rare LMNA missense mutation causing a severe phenotype of mandibuloacral dysplasia type A: a case report
- Ichthyosis follicularis with alopecia and photophobia (IFAP): late diagnosis in 18‐year‐old man
- Hair That Is Difficult to Manage in a Hispanic Girl
- Acne-Associated Syndromes
- Monilethrix: the use of tricoscopy in clinical diagnosis
- Monilethrix: Beaded hair and hypotrichosis in a child
- Whole genome sequencing analysis of alpaca suggests TRPV3 as a candidate gene for the suri phenotype
- Painful thickened skin on the soles of the feet
- Dermatomyositis Disease in Dogs
- Central Centrifugal Cicatricial Alopecia (CCCA)
- Polycystic ovarian disease in adult and perimenopausal women
- Office Diagnosis of Hair Shaft Defects
- A missense mutation in the P2RY5 gene leading to autosomal recessive woolly hair in a Syrian patient
- Autosomal recessive hypotrichosis simplex with woolly hair: a report of a new family
- Sjogren-Larsson syndrome
- Woolly Hair in Two Siblings
- The medusa head: Dermoscopic diagnosis of woolly hair syndrome
- A homozygous nonsense mutation identified in <i>COL7A1</i> in a family with autosomal recessive dystrophic epidermolysis bullosa
- Whole-genome SNP genotyping mapped a novel locus for hereditary hypotrichosis on chromosome 2q31.1–q32.2
- Clomiphene Citrate versus Letrozole for Ovulation Induction in PCOS: A Comparative Study
- Advances in the treatment of autosomal recessive congenital ichthyosis, a look towards the repositioning of drugs
- Case report: Heterozygous mutation in HTRA1 causing typical cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy
- An autosomal recessive nonsense variant in the EGFR gene induces perinatal lethality in “Blonde d'Aquitaine” calves
- Defolliculated (Dfl): A Dominant Mouse Mutation Leading to Poor Sebaceous Gland Differentiation and Total Elimination of Pelage Follicles
- Severe Monilethrix Associated with Intractable Scalp Pruritus, Posterior Subcapsular Cataract, Brachiocephaly, and Distinct Facial Features: A New Variant of Monilethrix Syndrome?
- Genetics of Inherited Ichthyoses and Related Diseases
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- Asebia-2J (Scd1ab2J): A New Allele and a Model for Scarring Alopecia
- Mutations in the vitamin D receptor and hereditary vitamin D-resistant rickets