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Results of search for 'au:"Gu, Xue Fan"', page 1 of 4
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Authors
Gao, Xiao-Lan
Gao, Xiao-lan
Gong, Zhu-Wen
Gu, Xue-Fan
Gu, Xue-fan
Han, Bei
Han, Lian-Shu
Han, Lian-shu
Huang, Zhuo
Jin, Jing
Li, Xiao-yan
Qiu, Wen-Juan
Qiu, Wen-juan
Wang, Yu
Ye, Jun
Zhang, Hui-Wen
Zhang, Hui-wen
Zhang, Ya-Fen
Zhang, Ya-fen
Zhou, Jian-de
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Adolescent
Adult
Asian People
Base Sequence
Child
Child, Preschool
China
DNA Mutational Analysis
Female
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Infant, Newborn
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Mutation
Phenylketonurias
Tandem Mass Spectrometry
analogs & derivatives
blood
diagnosis
genetics
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Your search returned 77 results.
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1.
[Present status and trends of prevention and treatment of lysosomal storage diseases].
[electronic resource]
by
Gu, Xue-fan
Producer:
20101202
In:
Zhonghua er ke za zhi = Chinese journal of pediatrics
vol. 46
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2.
[History and prospect of the neonatal screening program for inborn errors of metabolism].
[electronic resource]
by
Gu, Xue-fan
Producer:
20100504
In:
Zhonghua er ke za zhi = Chinese journal of pediatrics
vol. 43
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3.
A study of gene expression profiles of cultured embryonic rat neurons induced by phenylalanine.
[electronic resource]
by
Zhang, Huiwen
Gu, Xue Fan
Producer:
20050728
In:
Metabolic brain disease
vol. 20
Online resources:
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4.
Newborn screening of inherited metabolic diseases by tandem mass spectrometry.
[electronic resource]
by
Yu, Chun-li
Gu, Xue-fan
Producer:
20140428
In:
Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences
vol. 38
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5.
[The lab diagnosis of Gaucher disease should be pay more attention].
[electronic resource]
by
Zhang, Hui-wen
Gu, Xue-fan
Producer:
20100518
In:
Zhonghua yi xue za zhi
vol. 89
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6.
[Screening for phenylketonuria and congenital hypothyroidism in 5.8 million neonates in China].
[electronic resource]
by
Gu, Xue-fan
Wang, Zhi-guo
Producer:
20040708
In:
Zhonghua yu fang yi xue za zhi [Chinese journal of preventive medicine]
vol. 38
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7.
[Alteration of gene expression profiles of cultured embryo rat cortex induced by phenylalanine].
[electronic resource]
by
Zhang, Hui-Wen
Gu, Xue-Fan
Producer:
20040722
In:
Sheng li xue bao : [Acta physiologica Sinica]
vol. 56
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8.
[Both social and economic benefits should be considered simultaneously in prevention and treatment of hereditary metabolic diseases].
[electronic resource]
by
Gu, Xue-fan
Han, Lian-shu
Ye, Jun
Producer:
20100525
In:
Zhonghua er ke za zhi = Chinese journal of pediatrics
vol. 43
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9.
[Double stranded RNA (RNA interference RNAi) in different creatures].
[electronic resource]
by
Han, Bei
Wang, Xiu-Min
Gu, Xue-Fan
Producer:
20051017
In:
Yi chuan = Hereditas
vol. 24
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10.
[Prenatal diagnosis of mucopolysaccharidosis type II].
[electronic resource]
by
Zhang, Xin-shun
Zhang, Hui-wen
Gu, Xue-fan
Producer:
20111209
In:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
vol. 28
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11.
[Prenatal diagnosis of congenital adrenal hyperplasia in a case].
[electronic resource]
by
Xu, Shan-shan
Liao, Xiang-yun
Gu, Xue-fan
Producer:
20101222
In:
Zhonghua er ke za zhi = Chinese journal of pediatrics
vol. 45
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12.
[Technique of PCR-ACRS for the detection of CYP21 gene mutations].
[electronic resource]
by
Liao, Xiang-yun
Zhang, Ya-fen
Gu, Xue-fan
Producer:
20040114
In:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
vol. 20
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13.
[CYP21 gene point mutations study in 21-hydroxylase deficiency patients].
[electronic resource]
by
Liao, Xiang-yun
Zhang, Ya-fen
Gu, Xue-fan
Producer:
20040512
In:
Zhonghua er ke za zhi = Chinese journal of pediatrics
vol. 41
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14.
[Effect of phenylalanine on genes expression of Rho GTPases: possible relevance to neuron damage induced by phenylalanine].
[electronic resource]
by
Zhang, Yong-jun
Zhang, Hui-wen
Gu, Xue-fan
Producer:
20100511
In:
Zhonghua er ke za zhi = Chinese journal of pediatrics
vol. 43
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15.
[In vitro expression study of novel mutations in phenylalanine hydroxylase gene].
[electronic resource]
by
Zhang, Xin-shun
Gu, Xue-fan
Liang, Li-li
Producer:
20140327
In:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
vol. 30
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16.
[A novel mutation of the alpha-L-iduronidase gene in a patient with mucopolysaccharidosis type I].
[electronic resource]
by
Dou, Wei
Peng, Chao
Zheng, Jun-ke
Gu, Xue-fan
Producer:
20090327
In:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
vol. 24
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17.
[Detection of two novel mutations of iduronate-2-sulfatase gene in patients with mucopolysaccharidosis type II].
[electronic resource]
by
Dou, Wei
Peng, Chao
Zheng, Jun-Ke
Gu, Xue-Fan
Producer:
20090327
In:
Yi chuan = Hereditas
vol. 29
Online resources:
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18.
[Expression of green fluorescent protein vector by promoter sequence of CYP21 gene and CYP21P gene].
[electronic resource]
by
Han, Bei
Wang, Xiu-Min
Zhang, Ya-Fen
Gu, Xue-Fan
Producer:
20020703
In:
Yi chuan xue bao = Acta genetica Sinica
vol. 29
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19.
The oxidative molecular regulation mechanism of NOX in children with phenylketonuria.
[electronic resource]
by
He, Ying-Zhong
Gu, Xue-Fan
Lu, Li-Hua
Liang, Li-Li
Producer:
20150821
In:
International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience
vol. 38
Online resources:
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20.
[A discussion on risk factors of final height in 21-hydroxylase deficiency patients].
[electronic resource]
by
Han, Bei
Han, Lian-shu
Ye, Jun
Qiu, Wen-juan
Gu, Xue-fan
Producer:
20100607
In:
Zhonghua er ke za zhi = Chinese journal of pediatrics
vol. 42
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