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Adermatoglyphia
WES Gene Package Multiple Congenital Anomalie.Xlsx
Orphanet Report Series Rare Diseases Collection
Test Catalogue August 2019
An Update on the Biology and Management of Dyskeratosis Congenita and Related Telomere Biology Disorders
Genome-Wide Linkage Analysis and Whole-Genome Sequencing Identify a Recurrent SMARCAD1 Variant in a Unique Chinese Family with Basan Syndrome
Boards Fodder Disorders of Dyschromia (Hypo- and Hyperpigmentation) by Parin Pearl Rimtepathip, MD, and Janna Mieko Vassantachart, MD
WES Gene Package Multiple Congenital Anomalie.Xlsx
The Role of SMARCAD1 During Replication Stress Sarah Joseph
Whole Exome Sequencing Gene Package Multiple Congenital Anomaly, Version 8.1, 31-1-2020
TEST CATALOGUE October 2020 ACHIEVING a POSITIVE CHANGE
A Clinical Study on Genodermatoses and Their Effect On
Mendeliome Panel Versie V3 (4362 Genen) Centrum Voor Medische Genetica Gent
Hereditary Nonmelanoma Skin Cancer Vasiliki Nikolaou, MD,* Alexander J
A Mutation in a Skin-Specific Isoform of SMARCAD1 Causes Autosomal
Adermatoglyphia: Challenges and Prospects in Diagnosis
Dyskeratosis Congenita
Skin Disorders Panel Versie V4 (337 Genen) Centrum Voor Medische Genetica Gent
WES Gene Package Multiple Congenital Anomalie
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Help Me Understand Genetics
Meeting Program Commercial Support Future Annual As of April 15, 2014 Meetings 74Th Annual Meeting May 6-9, 2015 Hilton Atlanta Atlanta, Georgia
WES Gene Package Multiple Congenital Anomalie
Disqueratose Congénita Com Telómeros Curtos Numa Doente Do Sexo Feminino; Virgínia Vinha Zanuncio, Kelvin Oliveira Rocha
Dyskeratosis Congenita
Dyskeratosis Congenita with a Novel Genetic Variant in the DKC1 Gene
OMIM Mendelian Gene List V2.0
Orphanet Report Series Rare Diseases Collection