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- Case report: A novel splice-site mutation of MTX2 gene caused mandibuloacral dysplasia progeroid syndrome: the first report from China and literature review
- Cutaneous, Cranial, and Skeletal Defects in Children and Adults with Focal Dermal Hypoplasia
- A direct link between<i>Prss53</i>, hair curvature, and skeletal dysplasia
- Kallmann's syndrome: skeletal and psychological aspects of late diagnosis.
- Embryo‐Fetal Developmental Toxicity and Toxicokinetics Studies of YWS1903, a Novel Potassium‐Competitive Acid Blocker, in Pregnant Rats
- Becker’s Nevus Syndrome in a Pediatric Female Patient
- A Brazilian case of IFAP syndrome with severe congenital ichthyosis and limb malformations caused by a rare variant in MBTPS2
- Adverse Reactions to Oral Retinoids An Update
- Síndrome do nevo de Becker
- Dermatological drugs, topical agents, and cosmetics
- Teratogenic effect of isotretinoin in both fertile females and males (Review)
- Safety concerns of paternal drug exposure on fertility, pregnancy and offspring: An analysis based on the FDA adverse event reporting system
- Coordinating the Sculptors: Ectodysplasin-A (EDA) Signaling Cross-Talk with Skeletogenic Pathways
- Roles of Wnt7a in embryo development, tissue homeostasis, and human diseases
- WNT10B (wingless-type MMTV integration site family)
- The ITGB6 gene: its role in experimental and clinical biology
- Poster session
- Developmental and reproductive outcome of F1 generation of Wistar rats exposed to Acanthus montanus aqueous extract during organogenesis
- The use of a retinoid receptor antagonist in a new model to study vitamin A-dependent developmental events.
- Sildenafil: Looking Beyond Erectile Dysfunction: A Dermatological Perspective
- Perosomus elumbus fetal monster: a rare cause of dystocia in a beetal goat - a case report from Pakistan
- Making the head: Caspases in life and death
- Epidermal Nevi
- Ectodysplasin A (EDA) Signaling: From Skin Appendage to Multiple Diseases
- LATE-ONSET NEVUS COMEDONICUS IN AN ADULT PATIENT WITH DIABETES MELLITUS
- Congenital atrichia and hypotrichosis
- Congenital adrenal hyperplasia
- The rare association of congenital glaucoma, giant melanocytic nevus, alopecia, and hypospadias in an Egyptian child with neurofibromatosis type 1: a case report
- Nuclear Factor I-C Regulates TGF-β-dependent Hair Follicle Cycling*
- Skin and hair abnormalities of Cantu syndrome: A congenital hypertrichosis due to a genetic alteration mimicking the pharmacological effect of minoxidil