المؤلفون: Warner, E., Foulkes, W., Goodwin, P., Meschino, W., Blondal, J., Paterson, C., Ozcelik, H., Goss, P., Allingham-Hawkins, D., Hamel, N., Di Prospero, L., Contiga, V., Serruya, C., Klein, M., Moslehi, R., Honeyford, J., Liede, A., Glendon, G., Brunet, J.-S., Narod, S.

المصدر: JNCI Journal of the National Cancer Institute ; volume 91, issue 14, page 1241-1247 ; ISSN 0027-8874 1460-2105

الاتاحة: https://doi.org/10.1093/jnci/91.14.1241
http://academic.oup.com/jnci/article-pdf/91/14/1241/7795355/1241.pdf

المؤلفون: Malhotra A, Levine S, Allingham-Hawkins D

المصدر: Advances in Genomics and Genetics, Vol 2014, Iss default, Pp 115-128 (2014)

مصطلحات موضوعية: lcsh:Genetics, lcsh:QH426-470

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doajarticles::5e313893da00fc4ccdbaf5e6f4c08b07
http://www.dovepress.com/whole-exome-sequencing-for-cancer-ndash-is-there-evidence-of-clinical--peer-reviewed-article-AGG

المؤلفون: Suleiman, J., Allingham‐Hawkins, D., Hashem, M., Shamseldin, H.E., Alkuraya, F.S., El‐Hattab, A.W.

المصدر: Clinical Genetics ; volume 93, issue 2, page 360-364 ; ISSN 0009-9163 1399-0004

الاتاحة: http://dx.doi.org/10.1111/cge.13054
https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1111%2Fcge.13054
https://onlinelibrary.wiley.com/doi/pdf/10.1111/cge.13054

المؤلفون: Creighton, S, Almqvist, E W, MacGregor, D, Fernandez, B, Hogg, H, Beis, J, Welch, J P, Riddell, C, Lokkesmoe, R, Khalifa, M, MacKenzie, J, Sajoo, A, Farrell, S, Robert, F, Shugar, A, Summers, A, Meschino, W, Allingham-Hawkins, D, Chiu, T, Hunter, A, Allanson, J, Hare, H, Schween, J, Collins, L, Sanders, S, Greenberg, C, Cardwell, S, Lemire, E, MacLeod, P, Hayden, M R

المصدر: Clinical Genetics. 63(6):462-75

وصف الملف: print

URL الوصول: https://urn.kb.se/resolve?urn=urn:nbn:se:esh:diva-7513

المؤلفون: Suleiman, J., Allingham‐Hawkins, D., Hashem, M., Shamseldin, H. E., Alkuraya, F. S., El‐Hattab, A. W.

المصدر: Clinical Genetics; Feb2018, Vol. 93 Issue 2, p360-364, 6p, 1 Black and White Photograph, 1 Diagram, 1 Chart

مصطلحات موضوعية: INTELLECTUAL disabilities, QUADRIPLEGIA, EPILEPSY, NEURODEVELOPMENTAL treatment, HOMOZYGOSITY

المؤلفون: Holden, J.J.A., Percy, M., Allingham-Hawkins, D., Brown, W.T., Chiurazzi, P., Fish, G., Gane, L., Gunter, C., Hagerman, R., Jenkins, E.C., Kooy, Frank, Lubs, H.A., Murray, A., Neri, G., Schwartz, C., Tranebjaerg, L., Villard, L., Willems, P.J.

المصدر: 0148-7299 ; American journal of medical genetics

Relation: info:eu-repo/semantics/altIdentifier/isi/000079339300001

الاتاحة: https://hdl.handle.net/10067/258060151162165141

المؤلفون: Allingham-Hawkins, D J, Ray, P N

مصطلحات موضوعية: Male, congenital, hereditary, and neonatal diseases and abnormalities, X Chromosome, Base Sequence, Child, Preschool, Developmental Disabilities, Fragile X Syndrome, Intellectual Disability, Molecular Sequence Data, Humans, Polymerase Chain Reaction, Research Article, Repetitive Sequences, Nucleic Acid

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::2bd04dcfd42f2ffe72e16e0ee9384fa0
https://europepmc.org/articles/PMC1801229/

المؤلفون: Allingham-Hawkins, D. J., Tomkins, D. J.

المصدر: Somatic Cell and Molecular Genetics ; volume 17, issue 5, page 455-462 ; ISSN 0740-7750 1572-9931

الاتاحة: http://dx.doi.org/10.1007/bf01233169
http://link.springer.com/content/pdf/10.1007/BF01233169.pdf
http://link.springer.com/article/10.1007/BF01233169/fulltext.html
http://link.springer.com/content/pdf/10.1007/BF01233169