Unambiguous molecular detections with multiple genetic approach for the complicated chromosome 22q11 deletion syndrome

BACKGROUND: Chromosome 22q11 deletion syndrome (22q11DS) causes a developmental disorder during the embryonic stage, usually because of hemizygous deletions. The clinical pictures of patients with 22q11DS vary because of polymorphisms: on average, approximately 93% of affected individuals have a de...

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Detalles Bibliográficos
Autores principales: Yang, Chen, Huang, Cheng-Hung, Cheong, Mei-Leng, Hung, Kun-Long, Lin, Lung-Huang, Yu, Yeong-Seng, Chien, Chih-Cheng, Huang, Huei-Chen, Chen, Chan-Wei, Huang, Chi-Jung
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2656481/
https://www.ncbi.nlm.nih.gov/pubmed/19243607
http://dx.doi.org/10.1186/1471-2350-10-16

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2656481/
https://www.ncbi.nlm.nih.gov/pubmed/19243607
http://dx.doi.org/10.1186/1471-2350-10-16

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