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- Loss of a homologous group of proteins in a dominantly inherited ectodermal malformation
- Disruption of the temporally regulated cloaca endodermal β-catenin signaling causes anorectal malformations
- Ichthyosis with confetti: clinics, molecular genetics and management
- The Phenotypic and Genotypic Spectra of Ichthyosis With Confetti Plus Novel Genetic Variation in the 3′ End of<i>KRT10</i>
- Omenn syndrome in a 10-month-old male with athymia and VACTERL association
- Ectodysplasin A (EDA) Signaling: From Skin Appendage to Multiple Diseases
- Cutaneous, Cranial, and Skeletal Defects in Children and Adults with Focal Dermal Hypoplasia
- Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements
- Hair shaft structures in EDAR induced ectodermal dysplasia
- Morpho-Regulation of Ectodermal Organs
- Congenital atrichia and hypotrichosis
- Stimulation of ectodermal organ development by Ectodysplasin-A1
- Mammalian-specific ectodermal enhancers control the expression of <i>Hoxc</i> genes in developing nails and hair follicles
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Hair and Nail Relationship
- Expression ofWise in chick embryos
- A TP63 Mutation Causes Prominent Alopecia with Mild Ectodermal Dysplasia
- Use of chemotherapy during human pregnancy
- Biology and Genetics of Hair
- Orai1 expression pattern in tooth and craniofacial ectodermal tissues and potential functions during ameloblast differentiation
- Inherited Disorders of the Hair
- Rapp-Hodgkin syndrome: A review of the aspects of hair and hair color
- Epidermal stem cell fate: what can we learn from embryonic stem cells?
- ADULT (acro–dermato–ungual–lacrimal–tooth) syndrome: A case report from India
- Current Genetics in Hair Diseases
- A case of <i>MBTPS1</i>‐related disorder due to compound heterozygous variants in <i>MBTPS1</i> gene: Genotype–phenotype expansion and the emergence of a novel syndrome
- Clinical Case Notes. Retinoblastoma, microphthalmia and the chromosome 13q deletion syndrome
- WNT10B (wingless-type MMTV integration site family)
- Further Insights in Trichothiodistrophy: A Clinical, Microscopic, and Ultrastructural Study of 20 Cases and Literature Review
- Making the head: Caspases in life and death