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. Author manuscript; available in PMC: 2016 Apr 1.
Published in final edited form as: Birth Defects Res A Clin Mol Teratol. 2015 Mar 16;103(4):276–283. doi: 10.1002/bdra.23362

Table 1.

Locations (hg18) and sizes of the two genomic regions on chromosomes 7q34 (upper row) and 8p11 (lower row) that showed the most significant over-transmission of the allele with the missing DNA segment from a hemizygous parent to an offspring, comparing trios with affected probands to control trios. These regions overlapped with the MGAM gene (chromosome 7), and ADAM3A / ADAM5 (chromosome 8), respectively.

chr start end size genes
7 141,380,317 141,447,476 67.2 kb MGAM
8 39,341,981 39,548,228 206.2 kb ADAM3A, ADAM5