Application of multiplex ligation-dependent probe amplification, and identification of a heterozygous Alu-associated deletion and a uniparental disomy of chromosome 1 in two patients with 3-hydroxy-3-methylglutaryl-CoA lyase deficiency.
about
Application of multiplex ligation-dependent probe amplification, and identification of a heterozygous Alu-associated deletion and a uniparental disomy of chromosome 1 in two patients with 3-hydroxy-3-methylglutaryl-CoA lyase deficiency.
description
2015 nî lūn-bûn
@nan
2015年の論文
@ja
2015年論文
@yue
2015年論文
@zh-hant
2015年論文
@zh-hk
2015年論文
@zh-mo
2015年論文
@zh-tw
2015年论文
@wuu
2015年论文
@zh
2015年论文
@zh-cn
name
Application of multiplex ligat ...... glutaryl-CoA lyase deficiency.
@ast
Application of multiplex ligat ...... glutaryl-CoA lyase deficiency.
@en
type
label
Application of multiplex ligat ...... glutaryl-CoA lyase deficiency.
@ast
Application of multiplex ligat ...... glutaryl-CoA lyase deficiency.
@en
prefLabel
Application of multiplex ligat ...... glutaryl-CoA lyase deficiency.
@ast
Application of multiplex ligat ...... glutaryl-CoA lyase deficiency.
@en
P2093
P2860
P356
P1476
Application of multiplex ligat ...... glutaryl-CoA lyase deficiency.
@en
P2093
Hiroko Kouzan
Katsuaki Ohara
Mika Ishige
Naomi Sakaguchi
Toju Tanaka
Tomoko Ichihara
Toshiyuki Fukao
Toshiyuki Yamamoto
Yasutomi Kinosada
Yuka Aoyama
P2860
P304
P356
10.3892/IJMM.2015.2184
P577
2015-04-14T00:00:00Z