C - Chemistry – Metallurgy – 12 – Q
Patent
C - Chemistry, Metallurgy
12
Q
C12Q 1/68 (2006.01)
Patent
CA 2116633
The invention relates to method for the genotype diagnosis of FHM, by searching the presence of a mutated gene responsible for the disease, comprising the search of the presence of a mutation responsible for FHM on the chromosome 19, in the region of it comprised between the microsatellites D19S216 and D19S215, of a family or of an at risk individual, including foetus.
Joutel Anne Marie Gisele
Tournier-Lasserve Elisabeth Andree
Van Effenterre Nee Bousser Marie-Germaine Madeleine Jeanne
Fetherstonhaugh & Co.
Institut National de La Sante Et de La Recherche Medicale (inser
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