Microcephalic osteodysplastic primordial dwarfism type ii: Report of three cases and review
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference18 articles.
1. Wolcott-Rallison syndrome
2. Osteodysplastic primordial dwarfism type ii with normal intellect but delayed central nervous system myelination
3. Microcephalic osteodysplastic primordial dwarfism, type II
Cited by 43 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. Clinical Findings and Dental Manifestations Associated With Microcephalic Osteodysplastic Primordial Dwarfism Type II: A Case Report;Journal of Pediatrics Review;2022-10-01
2. A 10-Year-Old Boy with Short Stature and Microcephaly, Diagnosed with Moyamoya Syndrome and Microcephalic Osteodysplastic Primordial Dwarfism Type II (MOPD II);American Journal of Case Reports;2021-11-09
3. A novel homozygous mutation of the PCNT gene in a Chinese patient with microcephalic osteodysplastic primordial dwarfism type II;Molecular Genetics & Genomic Medicine;2021-07-31
4. A Novel PCNT Frame Shift Variant (c.7511delA) Causing Osteodysplastic Primordial Dwarfism of Majewski Type 2 (MOPD II);Frontiers in Pediatrics;2020-06-25
5. Intracranial aneurysms in microcephalic primordial dwarfism: a systematic review;Journal of NeuroInterventional Surgery;2020-06-10
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