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1مورد إلكتروني
المصدر: The Journal of clinical endocrinology and metabolism, 97 (7
مصطلحات الفهرس: Endocrinologie, Child, Preschool, Consanguinity, DNA Mutational Analysis -- methods, Female, Genome, Human, Goiter -- diagnosis -- genetics, Homozygote, Humans, Hypothyroidism -- diagnosis -- genetics, Iodide Peroxidase -- analysis -- genetics, Male, Pedigree, Point Mutation -- physiology, Siblings, Young Adult, info:eu-repo/semantics/article, info:ulb-repo/semantics/articlePeerReview, info:ulb-repo/semantics/openurl/article
URL:
https://dipot.ulb.ac.be/dspace/bitstream/2013/144592/3/doi_128342.pdf http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/144592 http://worldcat.org/search?q=on:EQY+http://difusion-oai.ulb.ac.be/oai/request+DCG_ENTIRE_REPOSITORY+CNTCOLL -
2مورد إلكتروني
المصدر: Thyroid, 22 (9
مصطلحات الفهرس: Sciences bio-médicales et agricoles, Adult, Butadienes -- pharmacology, Carcinoma -- enzymology, Carcinoma, Papillary, Cell Line, Tumor, Child, Enzyme Inhibitors -- pharmacology, Female, Gene Expression Regulation, Neoplastic -- drug effects, Humans, Imidazoles -- pharmacology, Immunohistochemistry, Iodide Peroxidase -- analysis -- biosynthesis, MAP Kinase Signaling System -- drug effects -- physiology, Male, Middle Aged, Mutation, Nitriles -- pharmacology, Proto-Oncogene Proteins B-raf -- genetics, Pyridines -- pharmacology, Retrospective Studies, Thyroid Cancer, Papillary, Thyroid Neoplasms -- enzymology, Transforming Growth Factor beta1 -- metabolism, Young Adult, info:eu-repo/semantics/article, info:ulb-repo/semantics/articlePeerReview, info:ulb-repo/semantics/openurl/article
URL:
http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/318828 http://worldcat.org/search?q=on:EQY+http://difusion-oai.ulb.ac.be/oai/request+DCG_ENTIRE_REPOSITORY+CNTCOLL -
3مورد إلكتروني
المصدر: The Journal of clinical endocrinology and metabolism, 97 (7
مصطلحات الفهرس: Endocrinologie, Child, Preschool, Consanguinity, DNA Mutational Analysis -- methods, Female, Genome, Human, Goiter -- diagnosis -- genetics, Homozygote, Humans, Hypothyroidism -- diagnosis -- genetics, Iodide Peroxidase -- analysis -- genetics, Male, Pedigree, Point Mutation -- physiology, Siblings, Young Adult, info:eu-repo/semantics/article, info:ulb-repo/semantics/articlePeerReview, info:ulb-repo/semantics/openurl/article
URL:
https://dipot.ulb.ac.be/dspace/bitstream/2013/144592/3/doi_128342.pdf http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/144592 http://worldcat.org/search?q=on:EQY+http://difusion-oai.ulb.ac.be/oai/request+DCG_ENTIRE_REPOSITORY+CNTCOLL