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Figure 4 | BMC Medical Genetics

Figure 4

From: Detecting 22q11.2 deletion in Chinese children with conotruncal heart defects and single nucleotide polymorphisms in the haploid TBX1 locus

Figure 4

Positions of common variants of the 13 patients with 22q11.2 deletion. Ancestral alleles are written with small letters. The numerals from I to VIII are representative of the eight SNPs from rs5748417 to rs5746826, respectively. The corresponding identification numbers of the 13 patients with 22q11.2 deletions are listed at the left.

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BMC Medical Genetics

ISSN: 1471-2350

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