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Dive into the research topics where Gu Xf is active.

Publication


Featured researches published by Gu Xf.


Chinese journal of pediatrics | 2009

Analysis of gene mutations in Chinese patients with methylmalonic acidemia and homocysteinemia

Wang F; Han Ls; Hu Yh; Yang Yl; Ye J; Qiu Wj; Zhang Yf; Gao Xl; Wang Y; Gu Xf


Chinese journal of pediatrics | 2010

Clinical diagnosis and WISP3 gene mutation analysis for progressive pseudorheumatoid dysplasia

Ye J; Zhang Hw; Wang T; Cao Lf; Qiu Wj; Han Ls; Zhang Yf; Gu Xf


Chinese journal of pediatrics | 2004

A pilot study of selective screening for high risk children with inborn error of metabolism using tandem mass spectrometry in China

Gu Xf; Han Ls; Gao Xl; Yan Yl; Ye J; Qiu Wj


Chinese journal of pediatrics | 2013

Outcomes of patients with combined methylmalonic acidemia and homocystinuria after treatment

Huang Z; Han Ls; Ye J; Qiu Wj; Zhang Hw; Gao Xl; Wang Y; Ji Wj; Li Xy; Gu Xf


Chinese journal of pediatrics | 2004

Molecular genetic analysis of congenital lipoid adrenal hyperplasia

Qiu Wj; Ye J; Han B; Han Ls; Gu Xf


Chinese journal of pediatrics | 2009

Enzymatic diagnosis of 47 cases with mucopolysaccharidosis

Zhang Hw; Wang Y; Ye J; Qiu Wj; Han Ls; Gao Xl; Gu Xf


Chinese journal of pediatrics | 2010

[Establishment and clinical application of dried blood spots and mixed leukocytes for determination of acid alpha-glucosidase activity].

Qiu Wj; Wang X; Wang Y; Ye J; Han Ls; Zhang Hw; Gu Xf


Chinese journal of pediatrics | 2005

Screening and diagnosis of tetrahydrobiopterin responsive phenylalanine hydroxylase deficiency with tetrahydrobiopterin loading test

Zhang Zx; Ye J; Qiu Wj; Han Ls; Gu Xf


Chinese journal of pediatrics | 2016

[Applying multiplex ligation-dependent probe amplification in the diagnosis of 5 cases with ornithine transcarbamylase deficiency].

Gong Zw; Han Ls; Ye J; Qiu Wj; Zhang Hw; Yu Yg; Liang Ll; Gao Xl; Wang Y; Ji Wj; Gu Xf


Chinese journal of pediatrics | 2014

[Follow up and gene mutation analysis in cases suspected as 3-methylcrotonyl-coenzyme A carboxylase deficiency by neonatal screening].

Ye J; Gong L; Han Ls; Qiu Wj; Zhang Hw; Gao Xl; Jin J; Xu H; Gu Xf

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