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Research 271–300 of 1000+
- Autosomal recessive woolly hair/hypotrichosis with homozygous mutation in the <i>LIPH</i> gene: a case report
- Novel D323G mutation of <i>DSG4</i> gene in a girl with localized autosomal recessive hypotrichosis clinically overlapped with monilethrix
- Research Snippets
- The Use of High-Density SNP Array to Map Homozygosity in Consanguineous Families to Efficiently Identify Candidate Genes: Application to Woodhouse-Sakati Syndrome
- 314 Molecular genetic dissection of ILVEN leads to successful targeted therapy
- 190 Deficiency of the Human Cysteine Protease Inhibitor Cystatin M/E Causes Hypotrichosis and Dry Skin
- Whole-genome SNP genotyping mapped a novel locus for hereditary hypotrichosis on chromosome 2q31.1–q32.2
- SASH1 Mutations and Hereditary Disorders of Pigmentation: Review of Literature
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- Woolly Antics between the Sheaths
- Evaluation of hair structural abnormalities in children with different neurological diseases
- INDENTIFICATION OF GENES INVOLVED IN INHERITED ECTODERMAL DYSPLASIAS
- The systemic wrinkled skin phenotype involves aberrant expression and variation of genes related to the oxidative stress and extracellular matrix in Xiang pigs
- Natural variation in trichome density and biochemistry in Antirrhinum
- Mechanical forces in skin disorders
- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers
- CDH3 gene related hypotrichosis and juvenile macular dystrophy – A case with a novel mutation
- Congenital atrichia with papular lesions
- More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players
- A novel missense mutation in the mouse hairless gene causes irreversible hair loss: Genetic and molecular analyses of Hrm1Enu
- Congenital atrichia with papular lesions
- Hypotrichosis with juvenile macular dystrophy: a case report with molecular study
- Woolly hair generalizado: caso clínico e revisão da literatura
- Hypotrichosis with juvenile macular dystrophy: a case report with molecular study
- Biology and Genetics of Hair
- Variation in the caprine keratin-associated protein 15-1 (KAP15-1) gene affects cashmere fibre diameter
- HAIR LOSS IN WOMEN
- Multiorgan Dysfunction in a 7-Month-Old Boy With Developmental Delay and Poor Growth
- Case Report: Bi-allelic missense variant in the desmocollin 3 gene causes hypotrichosis and recurrent skin vesicles
- Inherited Acrodermatitis Enteropathica