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A Forabosco

Showing results (131-140 of 134) with videos related to

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Human Mutation|January 1, 1992
Two transthyretin variants (TTR Ala-49 and TTR Gln-89) in two Sicilian kindreds with hereditary amyloidosisM R Almeida, A Ferlini, A Forabosco, et al.
Journal of Immunogenetics|October 1, 1981
Serum immunoglobulins and lymphocyte subpopulations derangement in Turner's syndromeE Cacciari, M Masi, M P Fantini, et al.
Human Mutation|February 12, 2000
Mutation in the nerve-specific 5'non-coding region of Cx32 gene and absence of specific mRNA in a CMTX1 Italian family. Mutations in brief no. 195. OnlineL Flagiello, V Cirigliano, M Strazzullo, et al.
Journal of Medical Genetics|June 19, 2002
SHOX point mutations and deletions in Leri-Weill dyschondrosteosisC Falcinelli, L Iughetti, A Percesepe, et al.
Pageof 14

Showing results (131-140 of 134) with videos related to

Sort By:
Pageof 14
You have reached the last page of results.This site can display upto 134 results.
Human Mutation|January 1, 1992
Two transthyretin variants (TTR Ala-49 and TTR Gln-89) in two Sicilian kindreds with hereditary amyloidosisM R Almeida, A Ferlini, A Forabosco, et al.
Journal of Immunogenetics|October 1, 1981
Serum immunoglobulins and lymphocyte subpopulations derangement in Turner's syndromeE Cacciari, M Masi, M P Fantini, et al.
Human Mutation|February 12, 2000
Mutation in the nerve-specific 5'non-coding region of Cx32 gene and absence of specific mRNA in a CMTX1 Italian family. Mutations in brief no. 195. OnlineL Flagiello, V Cirigliano, M Strazzullo, et al.
Journal of Medical Genetics|June 19, 2002
SHOX point mutations and deletions in Leri-Weill dyschondrosteosisC Falcinelli, L Iughetti, A Percesepe, et al.
Pageof 14