المؤلفون: Mason, Lucy R., Green, Rhys E., Hirons, Graham J.M., Skinner, Andrew M.J., Peault, Stéphanie C., Upcott, Emily V., Wells, Erica, Wilding, David J., Smart, Jennifer

المصدر: In Journal for Nature Conservation December 2021 64

المؤلفون: Graham, J.M.

المصدر: 1999 International Symposium on Technology and Society - Women and Technology: Historical, Societal, and Professional Perspectives. Proceedings. Networking the World (Cat. No.99CH37005) Women and technology: historical, societal, and professional perspectives Technology and Society, 1999. Women and Technology: Historical, Societal, and Professional Perspectives. Proceedings. 1999 International Symposium on. :99-104 1999

Relation: 1999 International Symposium on Technology and Society - Women and Technology: Historical, Societal, and Professional Perspectives

المؤلفون: Fish, R.S., Graham, J.M., Loader, R.J.

المصدر: Proceedings. 24th EUROMICRO Conference (Cat. No.98EX204) EUROMICRO Euromicro Conference, 1998. Proceedings. 24th. 2:1029-1036 vol.2 1998

Relation: Proceedings 24th EUROMICRO Conference

المؤلفون: Graham, J.M., Caso, R.

المصدر: 32nd Annual Frontiers in Education Frontiers in education Frontiers in Education, 2002. FIE 2002. 32nd Annual. 2:F3B-F3B 2002

Relation: Proceedings of Conference on Frontiers in Education

المؤلفون: Graham, J.M., Caso, R., Rierson, J., Jong-Hwan Lee

المصدر: 32nd Annual Frontiers in Education Frontiers in education Frontiers in Education, 2002. FIE 2002. 32nd Annual. 2:F4B-F4B 2002

Relation: Proceedings of Conference on Frontiers in Education

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المؤلفون: Sobering, A.K., Bryant, L.M., Li, D., McGaughran, J., Maystadt, I., Moortgat, S., Graham, J.M., Haeringen, A. van, Ruivenkamp, C., Cuperus, R., Vogt, J., Morton, J., Brasch-Andersen, C., Steenhof, M., Hansen, L.K., Adler, E., Lyonnet, S., Pingault, V., Sandrine, M., Ziegler, A., Donald, T., Nelson, B., Holt, B., Petryna, O., Firth, H., McWalter, K., Zyskind, J., Telegrafi, A., Juusola, J., Person, R., Bamshad, M.J., Earl, D., Tsai, A.C.H., Yearwood, K.R., Marco, E., Nowak, C., Douglas, J., Hakonarson, H., Bhoj, E.J., Univ Washington Ctr Mendelian Geno

المصدر: Human Genetics and Genomics Advances, 3(3). ELSEVIER
Sobering, A K, Bryant, L M, Li, D, McGaughran, J, Maystadt, I, Moortgat, S, Graham, J M, van Haeringen, A, Ruivenkamp, C, Cuperus, R, Vogt, J, Morton, J, Brasch-Andersen, C, Steenhof, M, Hansen, L K, Adler, É, Lyonnet, S, Pingault, V, Sandrine, M, Ziegler, A, Donald, T, Nelson, B, Holt, B, Petryna, O, Firth, H, McWalter, K, Zyskind, J, Telegrafi, A, Juusola, J, Person, R, Bamshad, M J, Earl, D, Tsai, A C H, Yearwood, K R, Marco, E, Nowak, C, Douglas, J, Hakonarson, H, Bhoj, E J & University of Washington Center for Mendelian Genomics 2022, ' Variants in PHF8 cause a spectrum of X-linked neurodevelopmental disorders and facial dysmorphology ', Human Genetics and Genomics Advances, vol. 3, no. 3, 100102 . https://doi.org/10.1016/j.xhgg.2022.100102

مصطلحات موضوعية: histone demethylation, PHF8, Molecular Medicine, orofacial clefting, Genetics (clinical), epigenetic gene regulation, X-linked intellectual disability

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::56c0c2f4bddb24a1f74df42714cfbbe1
https://hdl.handle.net/1887/3561451

المؤلفون: Schirwani, S., Albaba, S., Carere, D.A., Sacoto, M.J. Guillen, Zamora, F. Milan, Si, Y., Rabin, R., Pappas, J., Renaud, D.L., Hauser, N., Reid, E., Blanchet, P., Foulds, N., Dixit, A., Fisher, R., Armstrong, R., Isidor, B., Cogne, B., Vergano, S. Schrier, Demirdas, S., Dykzeul, N., Cohen, J.S., Grand, K., Morel, D., Slavotinek, A., Albassam, H.F., Naik, S., Dean, J., Ragge, N., Cinzia, C., Tedesco, M.G., Harrison, R.E., Bouman, A., Palen, E., Challman, T.D., Willemsen, M.H., Vogt, J., Cunniff, C., Bergstrom, K., Walia, J.S., Bruel, A.L., Kini, U., Alkuraya, F.S., Slegesky, V., Meeks, N., Girotto, P., Johnson, D., Newbury-Ecob, R., Ockeloen, C.W., Prontera, P., Lynch, S.A., Li, D., Graham, J.M., Balasubramanian, M.

المساهمون: Clinical Genetics

المصدر: American Journal of Medical Genetics, Part A, 185(11), 3446-3458. Wiley-Liss Inc.
American Journal of Medical Genetics. Part A, 185, 3446-3458
American Journal of Medical Genetics. Part A, 185, 11, pp. 3446-3458

مصطلحات موضوعية: Adult, Male, Neurodevelopmental disorders Donders Center for Medical Neuroscience [Radboudumc 7], Adolescent, Hypertelorism, Developmental Disabilities, speech impairment, Genetic Variation, ASXL3, BRPS, Young Adult, Phenotype, ASXL3-related syndrome, Bainbridge–Ropers syndrome, Neurodevelopmental Disorders, intellectual disability, Child, Preschool, Mutation, Humans, Muscle Hypotonia, Female, Genetic Predisposition to Disease, Child, Transcription Factors

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::d43c121986c2a547dbd8f85e0da5f2b7
https://doi.org/10.1002/ajmg.a.62465

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