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- The mutational analysis of mitochondrial DNA in maternal inheritance of polycystic ovarian syndrome
- The inheritance of common baldness: Two B or not two B ?
- Alopecia Areata in a Pediatric Patient with Delayed Maternal Manifestation: A Case Report
- Genetic Variation in the Human Androgen Receptor Gene Is the Major Determinant of Common Early-Onset Androgenetic Alopecia
- Application of the basic and specific classification on patterned hair loss in Indians
- Early onset androgenetic alopecia in men and associated risk factors: a hospital based study
- Eruptive Vellus Hair Cyst
- Przewidywanie cech wyglądu człowieka na podstawie markerów DNA do celów medyczno-sądowych i kryminalistycznych
- Familial congenital generalized hypertrichosis
- A woman with iatrogenic androgenetic alopecia responding to finasteride
- Maternal androgen excess induces cardiac hypertrophy and left ventricular dysfunction in female mice offspring
- A Study on the Pattern of Genetic Inheritance of Polycystic Ovarian Syndrome
- Supplementary material from "Giant axonal neuropathy alters the structure of keratin intermediate filaments in human hair"
- Uncombable hair syndrome due to maternal uniparental disomy of chromosome 1
- Case Report: Compound heterozygous variants in LSS and TSPEAR genes causing hypotrichosis type 14 complicated with ectodermal dysplasia type 14
- Expanding the Clinical and Mutational Spectrum of Recessive AEBP1-Related Classical-Like Ehlers-Danlos Syndrome
- Familial hypotrichosis of the scalp. Autosomal dominant inheritance in four generations.
- Expanding the Senior-Løken syndrome spectrum: Combined Rothmund-Thomson features unveil the distinct Teelwani Syndrome phenotype
- Loose Anagen Hair as a Cause of Hereditary Hair Loss in Children
- Dissection of genetic variation and evidence for pleiotropy in male pattern baldness
- Congenital hypotrichosis due to short anagen
- Hereditary Hypotrichosis and Localized Morphea: A New Clinical Entity
- Pitfalls of mapping a large Turkish consanguineous family with vertical monilethrix inheritance.
- Transcriptome Sequencing and Mass Spectrometry Reveal Genes Involved in the Non-mendelian Inheritance-Mediated Feather Growth Rate in Chicken
- PSEUDOPELADE: AN INHERITED ALOPECIA
- Clouston syndrome: A complete genotype–Phenotype correlation after four decades and six generations
- Tracing selection signatures in the pig genome gives evidence for selective pressures on a unique curly hair phenotype in Mangalitza
- Relationship of a Novel c.429delC Deletion in Hairless Gene HR with Alopecia in Two Families from Southern Punjab, Pakistan
- Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome
- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers