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1Academic Journal
المؤلفون: Szafranski, P. (Przemyslaw), Dharmadhikari, A.V. (Avinash), Brosens, E. (Erwin), Gurha, P. (Priyatansh), Kołodziejska, K.E. (Katarzyna), Zhishuo, O. (Ou), Dittwald, P. (Piotr), Majewski, J. (Jacek), Mohan, K.N. (K. Naga), Chen, B.P.C. (Benjamin), Person, A.D. (Anthony), Tibboel, D. (Dick), Klein, J.E.M.M. (Annelies) de, Pinner, J. (Jason), Chopra PhD, M. (Mickey), Malcolm, G. (Girvan), Peters, G., Arbuckle, S. (Susan), Guiang III, S.F. (Sixto), Hustead, V.A. (Virginia), Jessurun, J. (Jose), Hirsch, R. (Russel), Witte, D. (David), Maystadt, I. (Isabelle), Sebire, N. (Neil), Fisher, R. (Rachel), Langston, C. (Claire), Sen, P. (Partha), Stankiewicz, P. (Paweł)
المصدر: Genome Research vol. 23 no. 1, pp. 22-33
Relation: http://repub.eur.nl/pub/61472; urn:hdl:1765/61472
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2Academic Journal
المؤلفون: Sen, P., Yang, Y., Navarro, C., Silva, I., Szafranski, P., Kolodziejska, K.E., Dharmadhikari, A.V., Mostafa, H., Kozakewich, H., Kearney, D., Cahill, J.B., Whitt, M., Bilic, M., Margraf, L., Charles, A., Goldblatt, J., Gibson, K., Lantz, P.E., Garvin, A.J., Petty, J., Kiblawi, Z., Zuppan, C., McConkie-Rosell, A., McDonald, M.T., Peterson-Carmichael, S.L., Gaede, J.T., Shivanna, B., Schady, D., Friedlich, P.S., Hays, S.R., Palafoll, I.V., Siebers-Renelt, U., Bohring, A., Finn, L.S., Siebert, J.R., Galambos, C., Nguyen, L., Riley, M., Chassaing, N., Vigouroux, A., Rocha, G., Fernandes, S., Brumbaugh, J., Roberts, K., Ho-Ming, L., Lo, I.F., Lam, S., Gerychova, R., Jezova, M., Valaskova, I., Fellmann, F., Afshar, K., Giannoni, E., Muhlethaler, V., Liang, J., Beckmann, J.S., Lioy, J., Deshmukh, H., Srinivasan, L., Swarr, D.T., Sloman, M., Shaw-Smith, C., van Loon, R.L., Hagman, C., Sznajer, Y., Barrea, C., Galant, C., Detaille, T., Wambach, J.A., Cole, F.S., Hamvas, A., Prince, L.S., Diderich, K.E., Brooks, A.S., Verdijk, R.M., Ravindranathan, H., Sugo, E., Mowat, D., Baker, M.L., Langston, C., Welty, S., Stankiewicz, P.
المصدر: Human mutation, vol. 34, no. 6, pp. 801-811
مصطلحات موضوعية: Amino Acid Sequence, Chromosome Mapping, Databases, Genetic, Female, Forkhead Transcription Factors/chemistry, Forkhead Transcription Factors/genetics, Forkhead Transcription Factors/metabolism, Gene Dosage, Gene Order, Humans, Infant, Newborn, Male, Molecular Sequence Data, Mutation, Open Reading Frames, Persistent Fetal Circulation Syndrome/genetics, Persistent Fetal Circulation Syndrome/metabolism, Persistent Fetal Circulation Syndrome/mortality, Persistent Fetal Circulation Syndrome/pathology, Protein Interaction Domains and Motifs/genetics, Sequence Alignment
وصف الملف: application/pdf
Relation: info:eu-repo/semantics/altIdentifier/pmid/23505205; info:eu-repo/semantics/altIdentifier/eissn/1098-1004; info:eu-repo/semantics/altIdentifier/urn/urn:nbn:ch:serval-BIB_FA8E13315D590; https://serval.unil.ch/notice/serval:BIB_FA8E13315D59; https://serval.unil.ch/resource/serval:BIB_FA8E13315D59.P001/REF.pdf
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3Academic Journal
المؤلفون: Sen, P., Yang, Y., Navarro, C., Silva, I., Szafranski, P., Kolodziejska, K.E., Dharmadhikari, A.V., Mostafa, H., Kozakewich, H., Kearney, D., Cahill, J.B., Whitt, M., Bilic, M., Margraf, L., Charles, A., Goldblatt, J., Gibson, K., Lantz, P.E., Garvin, A.J., Petty, J., Kiblawi, Z., Zuppan, C., McConkie-Rosell, A., McDonald, M.T., Peterson-Carmichael, S.L., Gaede, J.T., Shivanna, B., Schady, D., Friedlich, P.S., Hays, S.R., Palafoll, I.V., Siebers-Renelt, U., Bohring, A., Finn, L.S., Siebert, J.R., Galambos, C., Nguyen, L., Riley, M., Chassaing, N., Vigouroux, A., Rocha, G., Fernandes, S., Brumbaugh, J., Roberts, K., Ho-Ming, L., Lo, I.F., Lam, S., Gerychova, R., Jezova, M., Valaskova, I., Fellmann, F., Afshar, K., Giannoni, E., Muhlethaler, V., Liang, J., Beckmann, J.S., Lioy, J., Deshmukh, H., Srinivasan, L., Swarr, D.T., Sloman, M., Shaw-Smith, C., van Loon, R.L., Hagman, C., Sznajer, Y., Barrea, C., Galant, C., Detaille, T., Wambach, J.A., Cole, F.S., Hamvas, A., Prince, L.S., Diderich, K.E., Brooks, A.S., Verdijk, R.M., Ravindranathan, H., Sugo, E., Mowat, D., Baker, M.L., Langston, C., Welty, S., Stankiewicz, P.
المصدر: Serveur académique Lausannois ; Human Mutation, vol. 34, no. 6, pp. 801-811
Relation: urn:issn:1059-7794; 10670/1.hhqswg; https://serval.unil.ch/resource/serval:BIB_FA8E13315D59.P001/REF.pdf; http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_FA8E13315D590