لا يتم عرض هذه النتيجة على الضيوف.
تسجيل الدخول للوصول الكامل.

المؤلفون: Ramdas, Wishal D, Amin, Najaf, van Koolwijk, Leonieke M E, Janssens, A Cecile J W, Demirkan, Ayse, de Jong, Paulus T V M, Aulchenko, Yurii S, Wolfs, Roger C W, Hofman, Albert, Rivadeneira, Fernando, Uitterlinden, Andre G, Oostra, Ben A, Lemij, Hans G, Klaver, Caroline C W, Vingerling, Johannes R, Jansonius, Nomdo M, van Duijn, Cornelia M

المصدر: Journal of Medical Genetics; Mar2011, Vol. 48 Issue 3, p190-196, 7p, 3 Charts, 3 Graphs

المؤلفون: Arora, A, Minogue, P J, Liu, X, Addison, P K, Russel-Eggitt, I, Webster, A A, Hunt, D M, Ebihara, L, Beyer, E C, Berthoud, V M, Moore, A T

المصدر: Journal of Medical Genetics; Mar2008, Vol. 45 Issue 3, p155-160, 6p, 3 Color Photographs, 2 Black and White Photographs, 1 Chart

مصطلحات موضوعية: CONNEXINS, MEMBRANE proteins, CATARACT, EYE diseases, OPHTHALMOLOGY

المؤلفون: Tagariello, A., Heller, R., Greven, A., Kalscheuer, V. M., Molter, T., Rouch, A., Kress, W., Winterpocht, A.

المصدر: Journal of Medical Genetics; Jun2006, Vol. 43 Issue 6, p534-540, 7p, 1 Black and White Photograph, 4 Diagrams

مصطلحات موضوعية: HUMAN abnormalities, GENETIC disorders, SKULL, EXOPHTHALMOS, BRACHYCEPHALY, TOMOGRAPHY

المؤلفون: Dlugaszewska, B., Silahtaroglu, A., Menzel, C., Kübart, S., Cohen, M., Mundlos, S., Tümer, Z., Kjaer, K., Friedrich, U., Ropers, H-H., Tommerup, N., Neitzel, H., Kalscheuer, V. M.

المصدر: Journal of Medical Genetics; Feb2006, Vol. 43 Issue 2, p111-118, 8p, 1 Color Photograph, 1 Black and White Photograph, 2 Diagrams

مصطلحات موضوعية: HUMAN chromosome abnormalities, SYNDACTYLY, APERT syndrome, INTELLECTUAL disabilities, ECTOPIC hormones, PURE red cell aplasia, SCOLIOSIS

المؤلفون: Piluso, G., Politano, L., Aurino, S., Fanin, M., Ricci, E., Venfriglia, V. M., Belsito, A., Totaro, A., Saccone, V., Topaloglu, H., Nascimbeni, A. C., Fulizio, L., Broccolini, A., Canki-Klain, N., Comi, Li, Nigro, G., Angelini, C., Nigro, V.

المصدر: Journal of Medical Genetics; Sep2005, Vol. 42 Issue 9, p686-693, 8p, 1 Diagram, 4 Charts

مصطلحات موضوعية: CALPAIN, GENES, MUSCULAR dystrophy, GENETIC mutation, PHENOTYPES, GENETICS

لا يتم عرض هذه النتيجة على الضيوف.
تسجيل الدخول للوصول الكامل.

المؤلفون: Hellstrand, M., Danielsen, E. A., Steen, V. M., Ekman, A., Eriksson, E., Nilsson, C. L.

المصدر: Journal of Medical Genetics; Nov2004, Vol. 41 Issue 11, p867-871, 5p

مصطلحات موضوعية: GENETIC polymorphisms, SCHIZOPHRENIA, TARDIVE dyskinesia, GENETICS, HEREDITY

المؤلفون: Borg, I., Squire, M., Menzel, C., Stout, K., Morgan, D., Willatt, L., O'Brien, P. C. M., Ferguson-Smith, M. A., Ropers, H. H., Tommerup, N., Kalscheuer, V. M., Sargan, D. R.

المصدر: Journal of Medical Genetics; Jun2002, Vol. 39 Issue 6, p391-399, 9p, 3 Color Photographs, 1 Diagram, 4 Charts

مصطلحات موضوعية: AUTISM, GENE mapping, GENETICS, CHROMOSOMES, CHILD development, DEVELOPMENTAL disabilities

المؤلفون: Park, V M, Pivnick, E K

المصدر: Journal of Medical Genetics; Oct1998, Vol. 35 Issue 10, p813-820, 8p, 2 Black and White Photographs, 2 Charts, 2 Graphs