المؤلفون: Faivre, L, Collod-Beroud, G, Child, A, Callewaert, B, Loeys, B L, Binquet, C, Gautier, E, Arbustini, E, Mayer, K, Arslan-Kirchner, M, Stheneur, C, Kiotsekoglou, A, Comeglio, P, Marziliano, N, Halliday, D, Beroud, C, Bonithon-Kopp, C, Claustres, M, Plauchu, H, Robinson, P N, Adès, L, De Backer, J, Coucke, P, Francke, U, De Paepe, A, Boileau, C, Jondeau, G

مصطلحات موضوعية: Letters to JMG

وصف الملف: text/html

العلاقة: http://jmg.bmj.com/cgi/content/short/45/6/384Test; http://dx.doi.org/10.1136/jmg.2007.056382Test

الإتاحة: https://doi.org/10.1136/jmg.2007.056382Test
http://jmg.bmj.com/cgi/content/short/45/6/384Test

المؤلفون: Faivre, L, Collod-Beroud, G, Callewaert, B, Child, A, Binquet, C, Gautier, E, Loeys, B L, Arbustini, E, Mayer, K, Arslan-Kirchner, M, Stheneur, C, Kiotsekoglou, A, Comeglio, P, Marziliano, N, Wolf, J E, Bouchot, O, Khau-Van-Kien, P, Beroud, C, Claustres, M, Bonithon-Kopp, C, Robinson, P N, Adès, L, De Backer, J, Coucke, P, Francke, U, De Paepe, A, Jondeau, G, Boileau, C

المصدر: European Journal of Human Genetics ; volume 17, issue 4, page 491-501 ; ISSN 1018-4813 1476-5438

مصطلحات موضوعية: Genetics (clinical), Genetics

الإتاحة: https://doi.org/10.1038/ejhg.2008.207Test
http://www.nature.com/articles/ejhg2008207.pdfTest
http://www.nature.com/articles/ejhg2008207Test

المؤلفون: Klintschar, M., Bilkenroth, U., Arslan-Kirchner, M., Schmidtke, J., Stiller, D.

المصدر: International Journal of Legal Medicine ; volume 123, issue 1, page 55-58 ; ISSN 0937-9827 1437-1596

مصطلحات موضوعية: Pathology and Forensic Medicine

الإتاحة: https://doi.org/10.1007/s00414-008-0288-5Test

المؤلفون: Faivre, L., Collod-Beroud, G., Loeys, B.L., Child, A., Binquet, C., Gautier, E., Callewaert, B., Arbustini, E., Mayer, K., Arslan-Kirchner, M., Kiotsekoglou, A., Comeglio, P., Marziliano, N., Dietz, H.C., Halliday, D., Beroud, C., Bonithon-Kopp, C., Claustres, M., Muti, C., Plauchu, H., Robinson, P.N., Adès, L.C., Biggin, A., Benetts, B., Brett, M., Holman, K.J., De Backer, J., Coucke, P., Francke, U., De Paepe, A., Jondeau, G., Boileau, C.

المصدر: The American Journal of Human Genetics ; volume 81, issue 3, page 454-466 ; ISSN 0002-9297

مصطلحات موضوعية: Genetics (clinical), Genetics

الإتاحة: https://doi.org/10.1086/520125Test
https://api.elsevier.com/content/article/PII:S0002929707613433?httpAccept=text/xmlTest
https://api.elsevier.com/content/article/PII:S0002929707613433?httpAccept=text/plainTest

المؤلفون: Sheikhzadeh, S, Brockstaedt, L, Habermann, C R, Sondermann, C, Bannas, P, Mir, T S, Staebler, A, Seidel, H, Keyser, B, Arslan-Kirchner, M, Kutsche, K, Berger, J, Blankenberg, S, von Kodolitsch, Y

المساهمون: Institut für Humangenetik

مصطلحات موضوعية: info:eu-repo/classification/ddc

العلاقة: https://mediatum.ub.tum.de/1253586Test

الإتاحة: https://doi.org/10.1111/cge.12308Test
https://mediatum.ub.tum.de/1253586Test

المؤلفون: Sheikhzadeh, S., Brockstaedt, L., Habermann, C.R., Sondermann, C., Bannas, P., Mir, T.S., Staebler, A., Seidel, H., Keyser, B., Arslan‐Kirchner, M., Kutsche, K., Berger, J., Blankenberg, S., von Kodolitsch, Y.

المصدر: Clinical Genetics ; volume 86, issue 6, page 545-551 ; ISSN 0009-9163 1399-0004

الإتاحة: https://doi.org/10.1111/cge.12308Test

المؤلفون: Kleijer WJ, Garritsen VH, Linnebank M, Mooyer P, Huijmans JGM, Mustonen A, Simola KOJ, Arslan-Kirchner M, Battini R, Briones P, Cardo E, Mandel H, Tschiedl E, Wanders RJA and Koch HG

المساهمون: Kleijer, Wj, Garritsen, Vh, Linnebank, M, Mooyer, P, Huijmans, Jgm, Mustonen, A, Simola, Koj, Arslan-Kirchner, M, Battini, R, Briones, P, Cardo, E, Mandel, H, Tschiedl, E, Wanders RJA and Koch, Hg

العلاقة: info:eu-repo/semantics/altIdentifier/wos/WOS:000177969200008; volume:25; firstpage:399; lastpage:410; numberofpages:12; journal:JOURNAL OF INHERITED METABOLIC DISEASE; http://hdl.handle.net/11568/951103Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-0036746765

الإتاحة: http://hdl.handle.net/11568/951103Test

المؤلفون: Faivre, L, Collod-Beroud, G, Adès, L, Arbustini, E, Child, A, Callewaert, Bert, Loeys, Bart, Binquet, C, Gautier, E, Mayer, K, Arslan-Kirchner, M, Grasso, M, Beroud, C, Hamroun, D, Bonithon-Kopp, C, Plauchu, H, Robinson, P, De Backer, Julie, Coucke, Paul, Francke, U, Bouchot, O, Wolf, J, Stheneur, C, Hanna, N, Detaint, D, De Paepe, Anne, Boileau, C, Jondeau, G

المصدر: CLINICAL GENETICS ; ISSN: 0009-9163

مصطلحات موضوعية: Medicine and Health Sciences, Marfan syndrome, Ghent criteria, new criteria, nosology, WEILL-MARCHESANI-SYNDROME, PATHOGENIC FBN1 MUTATIONS, I FIBRILLINOPATHIES, DIAGNOSTIC-CRITERIA, ECTOPIA LENTIS, 1009 PROBANDS, GENE, TGFBR2, MANIFESTATIONS, HOMOGENEITY

وصف الملف: application/pdf

العلاقة: https://biblio.ugent.be/publication/2044822Test; http://hdl.handle.net/1854/LU-2044822Test; http://dx.doi.org/10.1111/j.1399-0004.2011.01703.xTest; https://biblio.ugent.be/publication/2044822/file/2044861Test

الإتاحة: https://doi.org/10.1111/j.1399-0004.2011.01703.xTest
https://biblio.ugent.be/publication/2044822Test
http://hdl.handle.net/1854/LU-2044822Test
https://biblio.ugent.be/publication/2044822/file/2044861Test

المؤلفون: Schwemmle, C., Arslan-Kirchner, M., Pabst, B., Ptok, M.

المصدر: HNO ; volume 60, issue 10, page 901-905 ; ISSN 0017-6192 1433-0458

مصطلحات موضوعية: Otorhinolaryngology

الإتاحة: https://doi.org/10.1007/s00106-011-2459-9Test

المؤلفون: Sheikhzadeh, S, Rybczynski, M, Habermann, C, Bernhardt, A, Arslan-Kirchner, M, Keyser, B, Kaemmerer, H, Mir, T, Staebler, A, Oezdal, N, Robinson, P, Berger, J, Meinertz, T, von Kodolitsch, Y

المساهمون: Klinik für Kinderkardiologie und angeborene Herzfehler (Prof. Hess)

مصطلحات موضوعية: info:eu-repo/classification/ddc

العلاقة: https://mediatum.ub.tum.de/1099702Test

الإتاحة: https://doi.org/10.1111/j.1399-0004.2010.01494.xTest
https://mediatum.ub.tum.de/1099702Test