PMC:2812425 / 4019-4444 JSONTXT

{"target":"https://pubannotation.org/docs/sourcedb/PMC/sourceid/2812425","sourcedb":"PMC","sourceid":"2812425","source_url":"https://www.ncbi.nlm.nih.gov/pmc/2812425","text":"Fig. 1 Pedigree and haplotypes of the HGF family under study. The proband, indicated by an arrow, has two affected and two unaffected children with four different partners. Haplotype analysis excluded the SOS1 gene at the GINGF1 locus as the disease gene in this family and narrowed the original 11.42-cM, 13.04-Mb GINGF3 locus, flanked by marker loci D2S2221 and D2S1788, down to the region between markers D2S220 and D2S352","divisions":[{"label":"label","span":{"begin":0,"end":6}}],"tracks":[]}