A Novel X-Linked Disorder of Immune Deficiency and Hypohidrotic Ectodermal Dysplasia Is Allelic to Incontinentia Pigmenti and Due to Mutations in IKK-gamma (NEMO)
Jonathan Zonana;Melissa E. Elder;Lynda C. Schneider;Seth J. Orlow.
American Journal of Human Genetics (2000)
Fibroblast growth factor receptor 3 ( FGFR3 ) transmembrane mutation in Crouzon syndrome with acanthosis nigricans
Gregory A. Meyers;Seth J. Orlow;Ian R. Munro;Kelly A. Przylepa.
Nature Genetics (1995)
Hay–Wells syndrome is caused by heterozygous missense mutations in the SAM domain of p63
John A. McGrath;Pascal H.G. Duijf;Volker Doetsch;Alan D. Irvine.
Human Molecular Genetics (2001)
Lines of Blaschko
Jean L. Bolognia;Seth J. Orlow;Sharon A. Glick.
Journal of The American Academy of Dermatology (1994)
Melanosomes Are Specialized Members of the Lysosomal Lineage of Organelles
Seth J. Orlow.
Journal of Investigative Dermatology (1995)
Large Congenital Melanocytic Nevi and the Risk for the Development of Malignant Melanoma: A Prospective Study
Ashfaq A. Marghoob;Sandra P. Schoenbach;Alfred W. Kopf;Seth J. Orlow.
Archives of Dermatology (1996)
Patient perspectives on the management of atopic dermatitis
Torsten Zuberbier;Seth J. Orlow;Amy S. Paller;Alain Taïeb.
The Journal of Allergy and Clinical Immunology (2006)
Increased risk of symptomatic hemangiomas of the airway in association with cutaneous hemangiomas in a “beard” distribution
Seth J. Orlow;Michael S. Isakoff;Francine Blei.
The Journal of Pediatrics (1997)
Evidence-Based Recommendations for the Diagnosis and Treatment of Pediatric Acne
Lawrence F. Eichenfield;Lawrence F. Eichenfield;Andrew C. Krakowski;Andrew C. Krakowski;Caroline Piggott;Caroline Piggott;James Del Rosso.
Neurocutaneous melanosis : clinical features of large congenital melanocytic nevi in patients with manifest central nervous system melanosis
Maria DeDavid;Seth J Orlow;Nathalie Provost;Ashfaq A Marghoob.
Journal of The American Academy of Dermatology (1996)
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