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Research 31–60 of 640
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- Anxiety in the Medically Ill: A Systematic Review of the Literature
- Acne Syndromes and Mosaicism
- Acne-Associated Syndromes
- Skin Development and Disease: A Molecular Perspective
- Ptosis in childhood
- Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: e-Posters
- Current Genetics in Hair Diseases
- Commonly associated disorders with complete scalp alopecia in early childhood: A review
- The Spectrum of Scarring in Craniofacial Wound Repair
- Effect of thyroid hormone and epidermal growth factor on tactile hair development and craniofacial morphogenesis in the postnatal rat.
- An Effective and Novel Technique for Hair Control in Craniofacial Surgery
- Familial aggregation of phenotypic expression of premature hair hypopigmentation in the craniofacial region
- The Fusion of Craniofacial Reconstruction and Microsurgery
- Factors affecting aesthetic results in patients undergoing craniofacial reconstruction following maxillofacial trauma
- Orai1 expression pattern in tooth and craniofacial ectodermal tissues and potential functions during ameloblast differentiation
- Lineage‐specific requirements of Alx4 function in craniofacial and hair development
- Advances and challenges in intravital imaging of craniofacial and dental progenitor cells
- <i>egfl6</i> expression in the pharyngeal pouch is dispensable for craniofacial development
- Palatogenesis and cutaneous repair: A two‐headed coin
- Teratogenic effect of isotretinoin in both fertile females and males (Review)
- Characterization of a mouse Scube3 reporter line
- Making the head: Caspases in life and death
- Developmental Plasticity of Patterned and Regenerating Oral Organs
- Cosmetic aspects of cranial reconstruction
- Novel frameshift mutation in TRPS1 in a ukrainian patient with trichorhinophalangeal syndrome type I
- Possible Role of Osteopathic Manipulation Treatment in Alleviation of Finasteride-Induced Dementia through Modulation of HOMER-3 Gene Methylation
- The use of a retinoid receptor antagonist in a new model to study vitamin A-dependent developmental events.
- Loss‐of‐function of Endothelin receptor type A results in Oro‐Oto‐Cardiac syndrome
- Cutaneous, Cranial, and Skeletal Defects in Children and Adults with Focal Dermal Hypoplasia