Infantile osteopetrosis, craniosynostosis, and Chiari malformation type I with novel OSTEM1 mutation
about
Closing the Gap: Genetic and Genomic Continuum from Syndromic to Nonsyndromic Craniosynostoses.Mutation Screening of Candidate Genes in Patients with Nonsyndromic Sagittal Craniosynostosis.Endoscopic third ventriculostomy for hydrocephalus in osteopetrosis: a case report and review of the literature.Case update on cranial osteopetrosis: which is the role of the neurosurgeon?
P2860
Infantile osteopetrosis, craniosynostosis, and Chiari malformation type I with novel OSTEM1 mutation
description
2013 nî lūn-bûn
@nan
2013年の論文
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2013年論文
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2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
2013年论文
@zh
2013年论文
@zh-cn
name
Infantile osteopetrosis, crani ...... e I with novel OSTEM1 mutation
@en
type
label
Infantile osteopetrosis, crani ...... e I with novel OSTEM1 mutation
@en
prefLabel
Infantile osteopetrosis, crani ...... e I with novel OSTEM1 mutation
@en
P2093
P2860
P356
P1476
Infantile osteopetrosis, crani ...... e I with novel OSTEM1 mutation
@en
P2093
A Al Jabri Abdullah
A H Mahmoud Adel
Faqeih Eissa
P2860
P356
10.4103/1817-1745.111420
P577
2013-01-01T00:00:00Z