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Research 61–90 of 1000+
- Adams–Oliver syndrome: new evidence in variable expressivity?
- Hair Anomalies in a 6-Year-Old Girl
- FOXN1 Deficiency: from the Discovery to Novel Therapeutic Approaches
- Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Loss of Msx2 Function Down-Regulates the FoxE3 Expression and Results in Anterior Segment Dysgenesis Resembling Peters Anomaly
- Secondary cicatricial and other permanent alopecias
- An infant with congenital micrognathia and upper airway obstruction was diagnosed as Hutchinson-Gilford progeria syndrome caused by a novel LMNA mutation: Case report and literature review
- Hormonal Therapy for Acne
- Genetic Defects of Female Sexual Differentiation
- Cutaneous manifestations of systemic infection in children
- Multiple congenital smooth muscle hamartoma: A case report
- SRD5A3 Is Required for Converting Polyprenol to Dolichol and Is Mutated in a Congenital Glycosylation Disorder
- WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes
- Position effect on <i>FGF13</i> associated with X-linked congenital generalized hypertrichosis
- What does acne genetics teach us about disease pathogenesis?
- Hair Loss in Children
- Dermatologic manifestations of endocrine disorders
- Le gène<i>hairless</i>de la souris
- Developmental Toxicity of Levo-Alpha-Acetylmethadol (LAAM) in Tolerant Rats
- NIPAL4 mutation c.527C˃A identified in Romanian patients with autosomal recessive congenital ichthyosis
- Adrenal causes of endocrine hypertension in childhood or adolescence
- Hair Loss in Children
- Modelling androgen synthesis and action during human sexual differentiation
- Platelet-rich Plasma Injection and Lipofilling-assisted Hair Transplantation on Residual Scalp Alopecia Post Aplasia Cutis Congenita Verticis (ACCV)
- Keratin 17 null mice exhibit age- and strain-dependent alopecia
- Polycystic Ovary Syndrome and Its Differential Diagnosis
- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle
- The Use of Human Dermal Papillae Conditioned Medium (HDPCM) on Aplasia Cutis Congenita in Lower Extremity due to Intrauterine Varicella Infection
- Trichoscopy of aplasia cutis congenita of the scalp in skin of color