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Pediatric Dermatology, ISSN 0736-8046, 09/2018, Volume 35, Issue 5, pp. 685 - 687
Journal Article
Orphanet Journal of Rare Diseases, ISSN 1750-1172, 02/2018, Volume 13, Issue 1, pp. 31 - 31
Background: Neurofibromatosis type 1 (NF1) is a genetic disorder characterized by a predisposition to develop multiple benign tumors. A major feature of NF1 is... 
Natural history study | Cutaneous neurofibromas | Neurofibromatosis type 1 | Random effect modeling | MEDICINE, RESEARCH & EXPERIMENTAL | CARBON-DIOXIDE LASER | GENETICS & HEREDITY | QUALITY-OF-LIFE | TUMORS | Care and treatment | Analysis | Neurofibromatosis | Clinical trials | Research | Diagnosis | Risk factors | Index Medicus
Journal Article
Pediatric Dermatology, ISSN 0736-8046, 11/2013, Volume 30, Issue 6, pp. e194 - e197
Journal Article
The Journal of Allergy and Clinical Immunology, ISSN 0091-6749, 04/2019, Volume 143, Issue 4, pp. 1482 - 1495
Journal Article
Human Mutation, ISSN 1059-7794, 2013, Volume 34, Issue 4, pp. 587 - 594
Journal Article
Journal Article
Journal Article
American Journal of Dermatopathology, ISSN 0193-1091, 2014, Volume 36, Issue 12, pp. e194 - e197
Journal Article
Dermatology Online Journal, ISSN 1087-2108, 2016, Volume 22, Issue 11
Atypical complete DiGeorge syndrome (DGS) is an extremely rare congenital disease characterized by an eczematous dermatitis, lymphadenopathy, and an... 
Neonatal rash | DiGeorge syndrome | Atypical complete DiGeorge syndrome | Eczematous eruption | Skin Diseases - etiology | Skin Diseases - diagnosis | DiGeorge Syndrome - diagnosis | DiGeorge Syndrome - complications | Humans | Infant | Male | Skin Diseases - pathology | Skin - pathology | Index Medicus
Journal Article
Journal of the American Academy of Dermatology, ISSN 0190-9622, 9/2010, Volume 63, Issue 3, pp. 440 - 447
Journal Article