Patterns of X chromosome inactivation in the rett syndrome-Reference-Cited by-同舟云学术

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Patterns of X chromosome inactivation in the rett syndrome

Published:1990-01 Issue:1 Volume:12 Page:131-135
ISSN:0387-7604
Container-title:Brain and Development
language:en
Short-container-title:Brain and Development

Author:

Zoghbi Huda Y,Percy Alan K,Schultz Rebecca J,Fill Carolyn

Publisher

Elsevier BV

Subject

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

Reference24 articles.

1. Über ein zerebral-atrophisches Syndrome bei Hyperammonämie;Rett,1966

2. A progressive syndrome of autism, dementia, ataxia, and loss of purposeful hand use in girls;Hagberg;Ann Neurol,1983

3. Rett syndrome-search for genetic markers;Hanefeld;Am J Med Genet,1986

4. Genetic aspects of Rett syndrome;Zoghbi;J Child Neurol,1988

5. X-linked dominant inherited diseases with lethality in hemizygous males;Wettke-Schafer;Hum Genet,1983

Cited by 115 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Distributed X chromosome inactivation in brain circuitry is associated with X-linked disease penetrance of behavior;Cell Reports;2024-04

2. Rett Syndrome and MECP2 Duplication Syndrome: Disorders of MeCP2 Dosage;Neuropsychiatric Disease and Treatment;2022-11

3. Analysis of X‐inactivation status in a Rett syndrome natural history study cohort;Molecular Genetics & Genomic Medicine;2022-03-23

4. MECP2 Mutations in the Rett Syndrome Patients from South India;Neurology India;2022-01

5. A rare case of a male child with post-zygotic de novo mosaic variant c.538C > T in MECP2 gene: a case report of Rett syndrome;BMC Neurology;2021-12

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