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Research 31–60 of 1000+
- Ulerythema ophryogenes with multiple congenital anomalies
- Keratin 17 Expression in the Hard Epithelial Context of the Hair and Nail, and its Relevance for the Pachyonychia Congenita Phenotype
- Congenital atrichia associated with nevus flammeus: A rare association
- Congenital atrichia associated with situs inversus and mesocardia
- Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia
- ĮGIMTA NERANDĖJANTI SKALPO ALOPECIJA: KLINIKINIS ATVEJIS IR DIFERENCINĖ DIAGNOSTIKA
- Secondary cicatricial and other permanent alopecias
- Le gène<i>hairless</i>de la souris
- FOXN1 Deficiency: from the Discovery to Novel Therapeutic Approaches
- Position effect on <i>FGF13</i> associated with X-linked congenital generalized hypertrichosis
- Mammalian-specific ectodermal enhancers control the expression of <i>Hoxc</i> genes in developing nails and hair follicles
- Clomiphene Citrate versus Letrozole for Ovulation Induction in PCOS: A Comparative Study
- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle
- Keratin 17 null mice exhibit age- and strain-dependent alopecia
- A case of congenital pili multigemini
- Congenital hypotrichosis due to short anagen
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2
- Netherton's syndrome: A syndrome of elevated IgE and characteristic skin and hair findings
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- The rare association of congenital glaucoma, giant melanocytic nevus, alopecia, and hypospadias in an Egyptian child with neurofibromatosis type 1: a case report
- Nevus psiloliparus: Newly described histopathological features from transverse sections
- PA33 When bones speak through nails: insights from a paediatric case series
- Cantú Syndrome Is Caused by Mutations in ABCC9
- Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome
- Human ClinicalPhenotype Associated with FOXN1 Mutations
- Germline Mutation in ATR in Autosomal- Dominant Oropharyngeal Cancer Syndrome
- Hair follicle dystrophy in a litter of domestic cats resembling lanceolate hair mutant mice
- Commonly associated disorders with complete scalp alopecia in early childhood: A review
- Contribution of Environmental Constituents in the Genomic Disruption of Cytokeratins
- Hedgehog Signaling, Keratin 6 Induction, and Sebaceous Gland Morphogenesis