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Article

New tetranucleotide STRP markers for detecting the 22q11.2 deletion.

Molecular and cellular probes - 1 Dec 2006

Yi Long, Xu Zheng-Feng, Mo Xu-Ming, Hu Ya-Li, Wang Dong-Jin, Han Bing, Wang Yong, Yang Chi, Jiang Yong-Zhong, Shen Li, Wu Xing, Zhu Rui-Fang, Zhou Xiao-Jun

Abstract excerpt

The 22q11.2 deletion syndrome is the most common microdeletion syndrome mainly characterized by hemizygous deletions and congenital heart defect (CHD). By using polymerase chain reaction (PCR), genotyping of short tandem repeat polymorphic (STRP) markers is a common and powerful means of detecting microdeletion. We have developed five new tetranucleotide repeat markers, 22D_4_1, 22D_4_2, 22D_4_3, 22D_4_4 and...

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PMID: 16774813
DOI: 10.1016/j.mcp.2006.03.008

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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