Search
for
Sort by
Research 31–60 of 1000+
- RNA sequencing reveals lncRNA-mediated non-mendelian inheritance of feather growth change in chickens
- Tracing selection signatures in the pig genome gives evidence for selective pressures on a unique curly hair phenotype in Mangalitza
- Siberian cats help in solving part of the mystery surrounding golden cats
- Cosmeceutical Treatments for Androgenetic Alopecia
- Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome
- A Heritable Keratinization Defect of the Superficial Epidermis in Norfolk Terriers
- Di-Genic Inheritance in Genodermatoses: Insights from Two Consanguineous Cases in a Reference Lebanese Center within the Middle East and North Africa (MENA) Region
- Study on related factors of AGA and efficacy of finasteride therapy in 201 patients
- The VEGF +405 G>C 5' untranslated region polymorphism and risk of PCOS: a study in the South Indian Women
- Ugreelig hår
- Clinical Findings, Cutaneous Pathology, and Response to Therapy in 21 Patients With Keratosis Pilaris Atrophicans
- Clouston syndrome: A complete genotype–Phenotype correlation after four decades and six generations
- Case Report: Compound heterozygous variants in LSS and TSPEAR genes causing hypotrichosis type 14 complicated with ectodermal dysplasia type 14
- Inherited Hairlessness: A Case Study of Familial Congenital Atrichia
- 17 beta-hydroxysteroid dehydrogenase 3 deficiency in the Mediterranean population.
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- The Genetics of Human Skin Disease
- Molecular Genetics of Keratinization Disorders – What’s New About Ichthyosis
- Expanding the Senior-Løken syndrome spectrum: Combined Rothmund-Thomson features unveil the distinct Teelwani Syndrome phenotype
- The genetics of androgenetic alopecia
- Ichthyosis Follicularis, Alopecia, and Photophobia Syndrome in a Saudi Child: A Case Report
- Inheritance of Some Electrophoretic Phenotypes of Human Hair
- Critical Evaluation of Concept of Genetics in Ayurveda WSR to Eight Undesired Body Types (Ashta Nindit)
- Development of polycystic ovary syndrome: involvement of genetic and environmental factors
- Pitfalls of mapping a large Turkish consanguineous family with vertical monilethrix inheritance.
- Keratosis follicularis spinulosa decalvans in a female
- Expanding the Clinical and Mutational Spectrum of Recessive AEBP1-Related Classical-Like Ehlers-Danlos Syndrome
- Alopezien und Hypotrichosen im Kindesalter
- Loose Anagen Syndrome: A Retrospective Chart Review of 37 Cases
- Multicentric calcified trichilemmal cysts with alopecia universalis affecting siblings