Jonghe, C. de

mutation disease patient family genet allele study alzheimer score region app 692 mutation cancer linkage carrier editor marker matter lesions analysis chromosome syndrome university letter haemorrhage hearing control model protein matter dementia amyloid 1555g mutation research frequency lesion subject department lod score genetic health group number testing result 318gly deafness hearing loss table insurance american society hearing impairment genotype individual preeclampsia assay glu 318gly memory sequence right blood figure institute cdo families phenotype american parent locus primer chromosome 7 ciliary triplet pathology association autosomal nos 3 gene defect neurofibrillary tangles 1555g function situs inversus mitochondrial