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Research 31–60 of 1000+
- A Splice Site Mutation in the Gene of the Human Type I Hair Keratin hHa1 Results in the Expression of a Tailless Keratin Isoform
- Genetic correlation by pedigree analysis in patients diagnosed with PCOS as per Rotterdam’s criteria
- Mutation detection of type II hair cortex keratin gene KRT86 in a Chinese Han family with congenital monilethrix
- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis
- Androgenetic alopecia: An autosomal dominant disorder
- Large Intragenic KRT1 Deletion Underlying Atypical Autosomal Dominant Keratinopathic Ichthyosis
- Autosomal Dominant Obstructive Sleep Apnea Syndrome Due to the New Variant c.980_984dup in COL1A2: A Case Report
- Heterozygous <i>KRT32</i> variant is responsible for autosomal dominant loose anagen hair syndrome
- An incompletely penetrant novel MAFB (p.Ser56Phe) variant in autosomal dominant multicentric carpotarsal osteolysis syndrome
- The inheritance of common baldness: Two B or not two B ?
- Monilethrix
- Moniletrix. Observación de esta infrecuente displasia pilosa en dos hermanos. Reporte clínico y dermatoscópico
- Recurrent E413K Mutation of hHb6 in a Japanese Family with Monilethrix
- Identification of a novel heterozygous mutation in the first Japanese case of Marie Unna hereditary hypotrichosis
- Alopezien und Hypotrichosen im Kindesalter
- Marie-unna hereditary hypotrichosis
- Pitfalls of mapping a large Turkish consanguineous family with vertical monilethrix inheritance.
- A New Clinical Variant of Hereditary Localized Alopecia: Report of a Chinese Family Mapped to Chromosome 2p25.1–2p23.2
- Ugreelig hår
- Hypotrichosis and Hair Loss on the Occipital Scalp
- Two females with hair loss
- Odd-Looking Hair and Progressive Alopecia in Mother and Son
- Informàtica i Dret penal: Els delictes relatius a la informàtica
- Novel<i>PAX</i><i>9</i>mutation associated with syndromic tooth agenesis
- Masquerading of trichotillomania in a family with monilethrix
- Hereditary Hypotrichosis and Localized Morphea: A New Clinical Entity
- Banded Scalp Hair with an Unusual Glistening Appearance in a Teenager: A Quiz
- Monilethrix – Case report of a rare disease
- Alopecia frontal fibrosante: revisão bibliográfica dos aspectos gerais, fisiopatológicos, diagnósticos e do tratamento
- Hereditary Mucoepithelial Dysplasia and Autosomal-Dominant IFAP Syndrome Is a Clinical Spectrum Due to SREBF1 Variants