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- The Genetics of Human Skin Disease
- Analogs of human genetic skin disease in domesticated animals
- Lichen planus pigmentosus and its variants: review and update
- Distinct mechanisms underlie pattern formation in the skin and skin appendages
- Quoi de neuf en dermatologie pédiatrique ?
- Viewpoint 1
- Phylloid terminal hair nevus: A unique clinical entity
- British Society for Paediatric Dermatology Annual Meeting, Sheffield, 18-19 November 2016
- Identification of somatic and germline mosaicism for a keratin 5 mutation in epidermolysis bullosa simplex in a family of which the proband was previously regarded as a sporadic case
- Focal Scalp Hair Heterochromia in an Infant
- Pigmentary mosaicism: An update
- Novel <i>RNF113A</i> Variant Underlying X‐Linked Trichothiodystrophy With Presumed Mosaicism in an Unaffected Mother
- A Clinical Genetics-Driven Dual Diagnosis of Prader–Willi Syndrome Due to Mosaic Maternal UPD(15) and NOTCH3-Related CADASIL
- A Mosaic Hotspot <i>PLCD1</i> Variant, Detectable in Blood‐Derived DNA, Associated With Nevus Trichilemmocysticus
- Embryologic layers in dermatology: Developmental checkpoint disorders, diagnostic insight, and regenerative futures
- Double-Lined Frontoparietal Scleroderma en coup de sabre
- Becker's nevus associated with chromosomal mosaicism and congenital adrenal hyperplasia
- CPC14 Blaschko-linear trichoepitheliomas: unveiling type 1 segmental mosaicism
- Porokeratotic adnexal ostial nevus: a paradigm of cutaneous mosaicism
- SUN-208 Rare Case of 47XXY/46XX Mosaic Klinefelter Syndrome
- Bullous Congenital Ichthyosiform Erythroderma with Tinea Capitis in Half-Siblings: Rare Phenomenon in Ichthyosis with Co-Existing Trichophyton rubrum Infection and Blocker Displacement Amplification for Mosaic Mutation Detection
- Segmental cherry angiomas associated with extragenital lichen sclerosus: A report of two cases
- Discordant phenotype in monozygotic twins with mosaic trisomy 12p in lymphocytes
- Genetic Defects of Female Sexual Differentiation
- What does acne genetics teach us about disease pathogenesis?
- Bloch-Sulzberger Syndrome: A Rare X-Linked Dominant Genetic Disorder in a Newborn
- Acne Syndromes and Mosaicism
- Phenotypic heterogeneity in human genetic diseases: ultrasensitivity-mediated threshold effects as a unifying molecular mechanism
- Modulating the stem cell niche for tissue regeneration
- The Rotterdam Study: 2018 update on objectives, design and main results