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vrk1 gene mutation test in two Chinese pedigrees of the first and second branchial arch syndrome / 临床耳鼻咽喉头颈外科杂志
Journal of Clinical Otorhinolaryngology Head and Neck Surgery ; (24): 1026-1028, 2007.
Article in Chinese | WPRIM | ID: wpr-747594
ABSTRACT
OBJECTIVE@#To explore the role of vrk1 gene in two Chinese pedigrees of the first and second branchial arch syndrome.@*METHOD@#Sixty members in 2 Chinese pedigrees were recruited. The exon 2 -13 were analyzed by polymerase chain reaction and direct sequencing.@*RESULT@#We found a new SNP in proband of Shandong pedigree.@*CONCLUSION@#vrk1 gene mutation can be excluded in 2 Chinese pedigrees of the first and second branchial arch syndrome.
Subject(s)
Full text: Available Index: WPRIM (Western Pacific) Main subject: Pedigree / Syndrome / Branchial Region / Exons / Protein Serine-Threonine Kinases / Asian People / Intracellular Signaling Peptides and Proteins / Genetics / Macrostomia / Mutation Limits: Female / Humans / Male Language: Chinese Journal: Journal of Clinical Otorhinolaryngology Head and Neck Surgery Year: 2007 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Pedigree / Syndrome / Branchial Region / Exons / Protein Serine-Threonine Kinases / Asian People / Intracellular Signaling Peptides and Proteins / Genetics / Macrostomia / Mutation Limits: Female / Humans / Male Language: Chinese Journal: Journal of Clinical Otorhinolaryngology Head and Neck Surgery Year: 2007 Type: Article