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. Author manuscript; available in PMC: 2018 May 29.
Published in final edited form as: Am J Med Genet. 1996 Oct 16;65(2):137–141. doi: 10.1002/(SICI)1096-8628(19961016)65:2<137::AID-AJMG11>3.0.CO;2-R

Fig. 7.

Fig. 7

PCR amplification with radio-labeled primers from MN1 locus (identified in the 3′ UTR region of the PAR-7 gene) from patient EE (middle lane), her mother (left lane) and her father (right lane). The mother showed two alleles (heterozygous) and the father showed one allele (homozygous) but for a different size allele. Patient EE shows only one allele from the mother and no allele from the father, thus a paternal deletion of the MN1 locus.