糖心vlog

Between Light and Dark, the Chimera Comes Out

Defective Lamellar Granule Secretion in Arthrogryposis, Renal Dysfunction, and Cholestasis Syndrome Caused by a Mutation in VPS33B

X-Linked Ectodermal Dysplasia With Immunodeficiency Caused by NEMO Mutation: Early Recognition and Diagnosis

• Editorial
  Molecular Genetics as a Diagnostic and Prognostic Aid in the Assessment of Neonates With Red, Scaly Genodermatoses: Work Still in Progress
  Suzanne E. Clements, MBChB, MRCP; John A. McGrath, MD, FRCP
  Arch Dermatol

Self-Healing Collodion Membrane and Mild Nonbullous Congenital Ichthyosiform Erythroderma Due to 2 Novel Mutations in the ALOX12B Gene

• Editorial
  Molecular Genetics as a Diagnostic and Prognostic Aid in the Assessment of Neonates With Red, Scaly Genodermatoses: Work Still in Progress
  Suzanne E. Clements, MBChB, MRCP; John A. McGrath, MD, FRCP
  Arch Dermatol
• Dermatology in the Postgenomic Era: Harnessing Human Variation for Personalized Medicine
  Anthony E. Oro, MD, PhD
  Arch Dermatol

Bullous Sweet Syndrome in a Patient With t(9;22)(q34;q11)-Positive Chronic Myeloid Leukemia Treated With the Tyrosine Kinase Inhibitor Nilotinib: Interphase Cytogenetic Detection of 叠颁搁-础叠尝鈥� Positive Lesional Cells

A Human Papillomavirus鈥揂ssociated Disease With Disseminated Warts, Depressed Cell-Mediated Immunity, Primary Lymphedema, and Anogenital Dysplasia: WILD Syndrome

鈥淣agashima-Type鈥� Keratosis as a Novel Entity in the Palmoplantar Keratoderma Category

• Editorial
  Recessive Palmoplantar Keratodermas: A Fertile Biological Hunting Ground
  Laurent Parmentier, MD, PhD; Peter M. Steijlen, MD, PhD; Maurice A. M. van Steensel, MD, PhD
  Arch Dermatol