PAX3 mutations and clinical characteristics in Chinese patients with Waardenburg syndrome type 1

Molecular Vision

Volumn 16, Issue , 2010, Pages 1146-1153

  Wang, Juan ^a   Li, Shiqiang ^a   Xiao, Xueshan ^a   Wang, Panfeng ^a   Guo, Xiangming ^a   Zhang, Qingjiong ^a  

^a SUN YAT SEN UNIVERSITY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

GENOMIC DNA; TRANSCRIPTION FACTOR PAX3;

ADULT; AMPLICON; ARTICLE; CHILD; CHINESE; CLINICAL FEATURE; CONTROLLED STUDY; ETHNIC DIFFERENCE; EYE COLOR; FEMALE; GENE DELETION; GENE FREQUENCY; GENE IDENTIFICATION; GENETIC ASSOCIATION; GENETIC CODE; GENETIC VARIABILITY; HETERODUPLEX ANALYSIS; HETEROTOPIA; HETEROZYGOTE; HUMAN; HUMAN CELL; INFANT; INTRON; MALE; MOLECULAR CLONING; MUTATIONAL ANALYSIS; NUCLEOTIDE SEQUENCE; PEDIGREE ANALYSIS; PHENOTYPE; POLYMERASE CHAIN REACTION; PRESCHOOL CHILD; PRIORITY JOURNAL; SCHOOL CHILD; SEQUENCE ANALYSIS; SINGLE STRAND CONFORMATION POLYMORPHISM; WAARDENBURG SYNDROME; WAARDENBURG SYNDROME TYPE 1;

ASIAN CONTINENTAL ANCESTRY GROUP; BASE SEQUENCE; CASE-CONTROL STUDIES; CHINA; DNA MUTATIONAL ANALYSIS; FAMILY; FEMALE; FUNDUS OCULI; HUMANS; MALE; MOLECULAR SEQUENCE DATA; MUTATION; PAIRED BOX TRANSCRIPTION FACTORS; PEDIGREE; PHENOTYPE; WAARDENBURG'S SYNDROME;

EID: 77955590811     PISSN: None     EISSN: 10900535     Source Type: Journal    
DOI: None     Document Type: Article

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