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Figure 1 | BMC Medical Genetics

Figure 1

From: Absence of mutations in NR2E1 and SNX3in five patients with MMEP (microcephaly, microphthalmia, ectrodactyly, and prognathism) and related phenotypes

Figure 1

Schematic drawing of 6q21 demonstrates relative positions of genes flanking SNX3. Green bar indicates location of breakpoint within intron 3 of SNX3 in patient with t(6;13)(q21;q12) translocation [3]. Red arrows indicate direction of transcription. Genetic locations of transcriptional start and end sites are from RefSeq genomic assembly NC_000006.10.

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BMC Medical Genetics

ISSN: 1471-2350

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