Delayed myelination in a patient with 18q- syndrome

Author:

Ono Jiro,Harada Koushi,Yamamoto Takehisa,Onoe Sachiko,Okada Shintaro

Publisher

Elsevier BV

Subject

Clinical Neurology,Developmental Neuroscience,Neurology,Pediatrics, Perinatology, and Child Health

Reference15 articles.

1. Deletion partielle des bras longs du chromosome 18;De Grouchy;Pathol Biol,1964

2. Syndromes associated with deletion of the long arm of chromosome 18 [del(18q)];Wilson;Am J Med Genet,1979

3. Neurologic manifestations in 18q- syndrome;Miller;Am J Med Genet,1990

4. Segmental spinal muscular atrophy and dermatological findings in a patient with chromosome 18q deletion;Weiss;Ann Neurol,1991

5. Molecular analysis of the 18q- syndrome—and correlation with phenotype;Kline;Am J Hum Genet,1993

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2. Abnormal Myelination in Ring Chromosome 18 Syndrome;Journal of Child Neurology;2012-01-30

3. High-field (9.4T) MRI of brain dysmyelination by quantitative mapping of magnetic susceptibility;NeuroImage;2011-06

4. C;Taybi and Lachman's Radiology of Syndromes, Metabolic Disorders and Skeletal Dysplasias;2007

5. Growth hormone benefits children with 18q deletions;American Journal of Medical Genetics Part A;2005

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