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Restrictive dermopathy
New ZMPSTE24 (FACE1) Mutations in Patients Affected with Restrictive
LMNA-Related Disorders
Early Onset Diabetes in Two Children Due to Progeria, a Monogenic Disease of DNA Repair
Werner and Hutchinson–Gilford Progeria Syndromes: Mechanistic Basis of Human Progeroid Diseases
Hutchinson-Gilford Progeria Syndrome—Current Status and Prospects for Gene Therapy Treatment
Outcomes of 4 Years of Molecular Genetic Diagnosis on a Panel Of
Lamin A/C Mechanotransduction in Laminopathies
Blueprint Genetics Progeria and Progeroid Syndromes Panel
Lamin a and ZMPSTE24 (FACE-1) Defects Cause Nuclear
Progeroid Laminopathy with Restrictive Dermopathy-Like Features Caused By
A Complex LINC Between Nuclear Envelope and Pathology
DNA Damage Responses in Progeroid Syndromes Arise from Defective Maturation of Prelamin A
Mutations in Patients Affected with Restrictive Dermopathy Or Related Progeroid Syndromes and Mutation Update
Review LAMINOPATHIES
Pilot Study Couple Recruitment, Triage and Reporting Plan
Mandibuloacral Dysplasia Type A-Associated Progeria Caused by Homozygous LMNA Mutation in a Family from Southern China
Newborndxtm Advanced Sequencing Evaluation Disorders List
Insights from Progeroid Syndromes Into Skin Cancer and Aging Brian C
Top View
Hallmarks of Progeroid Syndromes: Lessons from Mice and Reprogrammed Cells Dido Carrero, Clara Soria-Valles and Carlos López-Otıń*
Diagnosed Cases of Rare Diseases at CENTOGENE January 2012 to June 2016
Skin Disorders Panel Versie V4 (337 Genen) Centrum Voor Medische Genetica Gent
Analyses of LMNA-Negative Juvenile Progeroid Cases Confirms Biallelic
Expression of Disease-Causing Lamin a Mutants Impairs the Formation of DNA Repair Foci
Sclerodermalike Syndromes: the Great Imitator
Compound Heterozygous ZMPSTE24 Mutations Reduce Prelamin A
Prevalence and Incidence of Rare Diseases: Bibliographic Data
Prevalence and Incidence of Rare Diseases
Case Report of an Iraqi Patient with Progeria and Pulmonary Fibrosis
Restrictive Dermopathy: Report of Two Siblings
Myotonic Dystrophy—A Progeroid Disease?
Recessive Gene List V2.0