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Síndrome de Roussy-Levy
Frontiers | Molecular Mechanisms of the Genetic Predisposition to Acute Megakaryoblastic Leukemia in Infants With Down Syndrome
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Dominant Charcot–Marie–Tooth syndrome and cognate disorders - ScienceDirect
Roussy-Lévy syndrom - příznaky, projevy, symptomy - Příznaky a projevy nemocí
Spinal Muscular Atrophy, Distal, Autosomal Recessive, 5 disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials
Roussy–Lévy syndrome is a phenotypic variant of Charcot–Marie–Tooth syndrome IA associated with a duplication on chromosome 17p11.2 - ScienceDirect
Marijuana Psychosis: A Case Report* - Giampiero Bartolucci, Lawrence Fryer, Carlo Perris, Charles Shagass, 1969
Síndrome de Roussy-Lévy - Wikipedia, la enciclopedia libre
A Clinical Review of Charcot‐Marie‐Tooth - GARCIA - 1999 - Annals of the New York Academy of Sciences - Wiley Online Library
Roussy–Lévy syndrome is a phenotypic variant of Charcot–Marie–Tooth syndrome IA associated with a duplication on chromosome 17p11.2 - ScienceDirect
How To Say Dejerine-Roussy Syndrome - YouTube
Progressive Genetic-Metabolic Diseases of the Central Nervous System in Children | Pediatric Annals
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Roussy Levy syndrome - Getting a Diagnosis - Genetic and Rare Diseases Information Center
Hisham Shalaby MD, FRCS Ed (Tr & Orth) Consultant Orthopaedic Surgeon
Gustave Roussy • LITFL • Medical Eponym Library
Roussy-Levy Syndrome (disorder) | Semantic Scholar
Gustave Roussy • LITFL • Medical Eponym Library
Roussy–Lévy syndrome is a phenotypic variant of Charcot–Marie–Tooth syndrome IA associated with a duplication on chromosome 17p11.2 - ScienceDirect
PDF) The phenotypic manifestations of chromosome 17p11.2 duplication
Roussy-Lévy Syndrome
A practical approach to the genetic neuropathies | Practical Neurology
Progressive Genetic-Metabolic Diseases of the Central Nervous System in Children | Pediatric Annals
PMP22-related disease: A novel splice site acceptor variant and intrafamilial phenotype variability
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