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Showing results (21-30 of 23) with videos related to

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Human Mutation|March 25, 1999
Peutz-Jeghers syndrome: four novel inactivating germline mutations in the STK11 gene. Mutations in brief no. 227. OnlineR Kruse, S Uhlhaas, C Lamberti, et al.
Journal of Medical Genetics|September 18, 2007
High proportion of large genomic deletions and a genotype phenotype update in 80 unrelated families with juvenile polyposis syndromeS Aretz, D Stienen, S Uhlhaas, et al.
Journal of Medical Genetics|February 25, 1998
Peutz-Jeghers disease: most, but not all, families are compatible with linkage to 19p13.3S Olschwang, D Markie, S Seal, et al.
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Showing results (21-30 of 23) with videos related to

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Pageof 3
You have reached the last page of results.This site can display upto 23 results.
Human Mutation|March 25, 1999
Peutz-Jeghers syndrome: four novel inactivating germline mutations in the STK11 gene. Mutations in brief no. 227. OnlineR Kruse, S Uhlhaas, C Lamberti, et al.
Journal of Medical Genetics|September 18, 2007
High proportion of large genomic deletions and a genotype phenotype update in 80 unrelated families with juvenile polyposis syndromeS Aretz, D Stienen, S Uhlhaas, et al.
Journal of Medical Genetics|February 25, 1998
Peutz-Jeghers disease: most, but not all, families are compatible with linkage to 19p13.3S Olschwang, D Markie, S Seal, et al.
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