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Meleda disease
Keratosis Circumscripta Revisited: a Case Report and Review of the Literature
Mal De Meleda in a Taiwanese
WES Gene Package Multiple Congenital Anomalie.Xlsx
The First Reported Case of a Variant of Mal De Maleda of the Gamborg
(12) Patent Application Publication (10) Pub. No.: US 2010/0210567 A1 Bevec (43) Pub
Palmoplantar Keratoderma of the Gamborg-Nielsen Type Is Caused by Mutations in the SLURP1 Gene and Represents a Variant of Mal De Meleda
Towards a Comprehensive Resource for Elucidating the Pathogenesis of Inherited Keratodermas
Wo 2009/033735 A2
Keratinization Disorders and Genetic Aspects in Palmar and Plantar Keratodermas
Download CGT Exome V2.0
A CASE of MAL DE MELEDA DISEASE in CHITRADURGA - KARNATAKA Parvathi C
NGS Oncology)
Whole Exome Sequencing Gene Package Multiple Congenital Anomaly, Version 8.1, 31-1-2020
Genomeposter2009.Pdf
Urs-Schnyder-Lecture ESPD Dubrovnik Prof Dr. Dr. Judith Fischer
Aase–Smith Syndrome, 231 Abboud, M.R., 381 Abdallat Syndrome, 196
CV Bouadjar 2013
University of Birmingham Therapeutic Targeting of Cathepsin C
Top View
Northwestern University, October 2010
Newborndxtm Advanced Sequencing Evaluation Disorders List
Papillon-Lefevre Syndrome in 9 Year Old Peadatric Patient
Studies on Mendelian Disorders of Cornification
Skin Disorders Panel Versie V4 (337 Genen) Centrum Voor Medische Genetica Gent
WES Gene Package Multiple Congenital Anomalie
Hereditary Palmoplantar Keratoderma Associated with Primary (Congenital) Lymphedema
Mal De Meleda – Through History and Today
WES Gene Package Multiple Congenital Anomalie
1. Congenital Urea Cycle Disorders 2. Citrullinemia 3
Mal De Meleda
Genetic Linkage of Meleda Disease to Chromosome 8Qter
Mal De Meleda: a Report of Two Cases in One Family
Difuse Palmoplantar Keratoderma = تقرن الجلد الراحي الاخمصي المنتشر
A DSG1 Frameshift Variant in a Rottweiler Dog with Footpad Hyperkeratosis
The Role of Genetic Testing and Effect on Patient Care
Disease ID Disorder Name Gene Symbols OMIM ID