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
Dans Chinois
| 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.
Texte intégral:
Disponible
Indice:
WPRIM (Pacifique occidental)
Sujet Principal:
Pedigree
/
Syndrome
/
Région branchiale
/
Exons
/
Protein-Serine-Threonine Kinases
/
Asiatiques
/
Protéines et peptides de signalisation intracellulaire
/
Génétique
/
Macrostomie
/
Mutation
Limites du sujet:
Femelle
/
Humains
/
Mâle
langue:
Chinois
Texte intégral:
Journal of Clinical Otorhinolaryngology Head and Neck Surgery
Année:
2007
Type:
Article
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