Genetic and Rare Disease of the CNS. Part II: Holoprosencephaly (HPE)-Reference-Cited by-同舟云学术

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Genetic and Rare Disease of the CNS. Part II: Holoprosencephaly (HPE)

Published:2018-04-18 Issue:4 Volume:9 Page:626-627
ISSN:1948-7193
Container-title:ACS Chemical Neuroscience
language:en
Short-container-title:ACS Chem. Neurosci.

Author:

Lindsley Craig W.^ORCID

Publisher

American Chemical Society (ACS)

Subject

Cell Biology,Cognitive Neuroscience,Physiology,Biochemistry,General Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/acschemneuro.8b00135

Reference5 articles.

1. Embarking on a 5 Year Journey to Highlight Genetic and Rare Diseases of the Central Nervous System

2. Genetic and Rare Disease of the CNS. Part I: Fatal Familial Insomnia (FFI)

3. Holoprosencephaly: Clinical, anatomic, and molecular dimensions

4. The molecular genetics of holoprosencephaly

Cited by 4 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. Disorders of growth;Biochemical and Molecular Basis of Pediatric Disease;2021

2. A case of holoprosencephaly and a little review;Human Pathology: Case Reports;2019-03

3. Rare Disease Genomics and Clinical Diagnostics;Genomics and Clinical Diagnostics;2019-01-29

4. Digynic triploidy in a fetus presenting with semilobar holoprosencephaly;Taiwanese Journal of Obstetrics and Gynecology;2018-12

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