about
A p47-phox pseudogene carries the most common mutation causing p47-phox- deficient chronic granulomatous diseaseThe molecular biology, biochemistry, and physiology of human steroidogenesis and its disordersDuplication and positive selection among hominin-specific PRAME genes.Highly polymorphic XbaI RFLPs of the human 21-hydroxylase genes among Chinese.von Willebrand factor mutation enhancing interaction with platelets in patients with normal multimeric structure.Achondroplasia is defined by recurrent G380R mutations of FGFR3Detection of DNA sequence polymorphisms in human genomic DNA by using denaturing gradient gel blotsEvolutionary origin of mutations in the primate cytochrome P450c21 geneInfluence of aberrant observations on high-resolution linkage analysis outcomesSubstrate-dependent evolution of cytochrome P450: rapid turnover of the detoxification-type and conservation of the biosynthesis-type.Data on the 21-Hydroxylase deficient CAH patients and the identification of known/novel mutations in CYP21A2 gene.A de novo mutation in CYP21A2 gene in a case of in vitro fertilization.Hybrid survival motor neuron genes in patients with autosomal recessive spinal muscular atrophy: new insights into molecular mechanisms responsible for the disease.
P2860
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P2860
description
1990 nî lūn-bûn
@nan
1990 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
1990 թվականի հունիսին հրատարակված գիտական հոդված
@hy
1990年の論文
@ja
1990年論文
@yue
1990年論文
@zh-hant
1990年論文
@zh-hk
1990年論文
@zh-mo
1990年論文
@zh-tw
1990年论文
@wuu
name
Gene conversion in steroid 21-hydroxylase genes.
@ast
Gene conversion in steroid 21-hydroxylase genes.
@en
type
label
Gene conversion in steroid 21-hydroxylase genes.
@ast
Gene conversion in steroid 21-hydroxylase genes.
@en
prefLabel
Gene conversion in steroid 21-hydroxylase genes.
@ast
Gene conversion in steroid 21-hydroxylase genes.
@en
P2093
P2860
P1476
Gene conversion in steroid 21-hydroxylase genes
@en
P2093
P2860
P304
P407
P577
1990-06-01T00:00:00Z