about
Expression of the NYGGF4 gene during human preadipocyte differentiation and the regulative role of tumor necrosis factor-alphaAlternative splicing of RHAMM gene in chinese gastric cancers and its in vitro regulationRefined chromosome assignment of human novel H-RalGDS gene on chromosome 9q34.1 by using radiation hybrid genebridge 4 panelIdentification of a novel mutation IVS2-2A-->C of SEDL gene in a Chinese family with X-linked spondyloepiphyseal dysplasia tardaMutation and amplification of RIT1 gene in hepatocellular carcinomaInteraction between maternal periconceptional supplementation of folic acid and reduced folate carrier gene polymorphism of neural tube defectsTypes and frequencies of variants in Amelogenin gene in Chinese populationAssociation of thiazide-sensitive Na+-Cl* cotransporter gene polymorphisms with the risk of essential hypertensionAnalysis of acyl-coenzyme A: cholesterol acyltransferase 1 polymorphism in patients with endogenous hypertriglyceridemia in Chinese populationIncreased atria expression of receptor activity-modifying proteins in heart failure patientsAnalysis on FUT1 and FUT2 gene of 10 para-Bombay individuals in ChinaMutation analysis of the CHD7 gene in patients with congenital heart diseaseAssociation of polymorphism of the prostacyclin synthase gene with myocardial infarction in Uigur population of Xinjiang[The role of insulin-like growth factor-2 gene differentially methylated regions in TCDD-induced malformation][An evaluation for the function and significance concerned to alterations of P16 3D structure with gene mutation in esophageal squamous cell carcinoma].[Clinical and mutational features of maternal 3-methylcrotonyl coenzyme deficiency].[Analysis of a novel mutation of AR gene in a patient featuring mild androgen insensitivity syndrome].[In vitro expression and structural analysis of four missense mutations (G247S, E280G, P362T, A434D) of phenylalanine hydroxylase gene].[Sequence analysis of coding regions of KCNJ5 gene in unilateral adrenal hyperplasia].[Transglutaminase and neurodegenerative diseases].[Mutation analysis for a family affected with Charcot-Marie-Tooth disease type 4C].[Mutational analysis of SLC22A5 gene in eight patients with systemic primary carnitine deficiency].[Identification of a novel mutation of GALNS gene from a Chinese pedigree with mucopolysaccharidosis type IV A].[Mutation analysis of pathogenic genes in a Henan family affected with congenital stationary night blindness].[Strategies for exome sequence data analysis for discovering genes underlying autosomal recessive disorders].[Analysis of clinical features and GCDH gene mutations in four patients with glutaric academia type I].[Analysis of clinical data and genetic mutations in three Chinese patients with tyrosinemia type I].[Non-invasive prenatal diagnosis of Duchenne muscular dystrophy][Using the method of two-color fluorescence in situ hybridization to detect aneuploidy of human sperms][Cloning of the mouse Doc-1R gene by genomic walking][Cloning the 5 ' end fragment of ST13 cDNA by nested PCR][Isolating candidate inserted fragment from positive fused phage clones using quantitative PCR][Relationship between Line 1 methylation and clinical data of non-small cell lung cancer].[Clinical investigation and genetic analysis of a Chinese family with glutaric acidemia type I].A minidystrophin-EGFP fusion gene expressed in Cos-7 cells mediated by human source vector.[Cloning and tissue expression analysis of up-regulated cDNA fragment in human gastric cancer].[Molecular cloning of a novel gene located on chromosome 3p25.3 and an analysis of its expression in nasopharyngeal carcinoma][Molecular cloning of TSARG3 gene related to apoptosis in human spermatogenic cells].[Change of expression of cell/organs defense genes in brain tissue of rats with stroke-like episodes induced by complex environmental factors].[Study on a downstream signal molecule of human CASK/LIN-2].
P1433
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P1433
description
czasopismo naukowe
@pl
revista científica
@es
revue scientifique
@fr
rivista scientifica
@it
scientific journal
@en
wetenschappelijk tijdschrift
@nl
wissenschaftliche Fachzeitschrift
@de
науковий журнал
@uk
name
880-01 Zhonghua yi xue yi chua ...... se journal of medical genetics
@nl
Zhonghua yi xue yi chuan xue za zhi
@ast
Zhonghua yi xue yi chuan xue za zhi
@de
Zhonghua yi xue yi chuan xue za zhi
@en
Zhonghua yi xue yi chuan xue za zhi
@es
Zhonghua yi xue yi chuan xue za zhi
@fr
Zhonghua yi xue yi chuan xue za zhi
@it
type
label
880-01 Zhonghua yi xue yi chua ...... se journal of medical genetics
@nl
Zhonghua yi xue yi chuan xue za zhi
@ast
Zhonghua yi xue yi chuan xue za zhi
@de
Zhonghua yi xue yi chuan xue za zhi
@en
Zhonghua yi xue yi chuan xue za zhi
@es
Zhonghua yi xue yi chuan xue za zhi
@fr
Zhonghua yi xue yi chuan xue za zhi
@it
altLabel
Chinese Journal of Medical Genetics
@en
Zhonghua yixue yichuanxue zazhi
@en
prefLabel
880-01 Zhonghua yi xue yi chua ...... se journal of medical genetics
@nl
Zhonghua yi xue yi chuan xue za zhi
@ast
Zhonghua yi xue yi chuan xue za zhi
@de
Zhonghua yi xue yi chuan xue za zhi
@en
Zhonghua yi xue yi chuan xue za zhi
@es
Zhonghua yi xue yi chuan xue za zhi
@fr
Zhonghua yi xue yi chuan xue za zhi
@it
P1055
P1156
P1476
Chinese Journal of Medical Genetics
@en
Zhonghua yi xue yi chuan xue za zhi
@zh-cn