Zobrazeno 1 - 10
of 34
pro vyhledávání: '"Hoogeboom AJM"'
Autor:
Sharma, VP, Fenwick, AL, Brockop, MS, McGowan, SJ, Goos, JAC, Hoogeboom, AJM, Brady, AF, Jeelani, O, Lynch, SA, Mulliken, JB, Murray, DJ, Phipps, JM, Sweeney, E, Tomkins, SE, Wilson, LC, Bennett, S, Cornall, RJ, Broxholme, J, Kanapin, A, Donnelly, P, Johnson, D, Wall, SA, van der Spek, PJ, Mathijssen, IMJ, Maxson, RE, Twigg, SRF, Wilkie, AOM
Publikováno v:
LANCET. 381
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______1064::5d7fbbbd710bbe5cf64db4636f2945ba
http://ora.ox.ac.uk/objects/uuid:77a37a71-bbd9-4226-9e31-f65ade6fc9d2
http://ora.ox.ac.uk/objects/uuid:77a37a71-bbd9-4226-9e31-f65ade6fc9d2
Autor:
van Dooren, Marieke, Brooks, Alice, Hoogeboom, AJM, Hoonaard, TL, de Klein, Annelies, Wouters, Cokkie, Tibboel, Dick
Publikováno v:
American Journal of Medical Genetics, 127, 194-196. Wiley-Liss Inc.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=narcis______::a17b270e3d11b8e2ec4eb28dd271f8bd
https://pure.eur.nl/en/publications/6c365e52-b09c-41a6-9c32-e848a52cb4ac
https://pure.eur.nl/en/publications/6c365e52-b09c-41a6-9c32-e848a52cb4ac
Publikováno v:
Ultrasound in Obstetrics & Gynecology, 18, 378-383. John Wiley & Sons Ltd.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=narcis______::e8c5a75e5af2905f2c17ad2c71bd8671
https://pure.eur.nl/en/publications/420831d7-104c-4756-85c9-2ba91a21138f
https://pure.eur.nl/en/publications/420831d7-104c-4756-85c9-2ba91a21138f
Autor:
Haelst, Mieke, Hoogeboom, AJM, Galjaard, H, Kleijer, W, Hollander, NS, de Krijger, Ronald, Hennekam, RCM, Niermeijer, Martinus
Publikováno v:
American Journal of Medical Genetics, 104, 65-68. Wiley-Liss Inc.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=narcis______::ff7aef3833817645c8ac97f7d80fe44a
https://pure.eur.nl/en/publications/3f05b8f7-de05-4435-b216-e66c1554a899
https://pure.eur.nl/en/publications/3f05b8f7-de05-4435-b216-e66c1554a899
Publikováno v:
Ultrasound in Obstetrics & Gynecology, 17, 529-530. John Wiley & Sons Ltd.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=narcis______::5d6fa252d6e37191513f129919652107
https://pure.eur.nl/en/publications/e841438e-fe5a-4457-af6a-1ee4b9fa5212
https://pure.eur.nl/en/publications/e841438e-fe5a-4457-af6a-1ee4b9fa5212
Autor:
Galjaard, Robert-Jan, van der Ham, LI, Posch, NAS (Nicole), Dijkstra, PF, Oostra, Ben, Hovius, Steven, Timmenga, EJF, Sonneveld, GJ, Hoogeboom, AJM, Heutink, P
Publikováno v:
American Journal of Medical Genetics, 98, 256-262. Wiley-Liss Inc.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=narcis______::05a46de205c77d35a0dd72e282a38f52
https://pure.eur.nl/en/publications/9109fd7a-756b-49b5-ab43-c0f1dd04adb2
https://pure.eur.nl/en/publications/9109fd7a-756b-49b5-ab43-c0f1dd04adb2
Autor:
Haelst, Mieke, Brooks, Alice, Hoogeboom, AJM, Wessels, Marja, Tibboel, Dick, Jongste, Johan, Hollander, Jan, Bongers-Schokking, JJ, Niermeijer, Martinus, Willems, PJ
Publikováno v:
American Journal of Medical Genetics, 94, 170-173. Wiley-Liss Inc.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=narcis______::92f9c0b2d7295e261d0d5eed9abfa59d
https://pure.eur.nl/en/publications/dac919e4-c577-47d0-938b-fa2d8b29b53a
https://pure.eur.nl/en/publications/dac919e4-c577-47d0-938b-fa2d8b29b53a
Pfeiffer's syndrome resulting from an S351C mutation in the fibroblast growth factor receptor-2 gene
Autor:
Mathijssen, Irene, Vaandrager, JM (Michiel), Hoogeboom, AJM, Hesseling, A, van den Ouweland, Ans
Publikováno v:
Journal of Craniofacial Surgery, 9, 207-209. Lippincott Williams & Wilkins
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=narcis______::281275d464e6f7bc88b03b671356c101
https://pure.eur.nl/en/publications/276755a8-ea82-4106-8cdd-e19917e88922
https://pure.eur.nl/en/publications/276755a8-ea82-4106-8cdd-e19917e88922
Autor:
Hoogeboom, AJM, Govaerts, LCP, Niermeijer, Martinus, van den Bosch, W.J.H.M., Büller, H.A., van der Does, E., de Jong, R., Sukhai, R.N.
Publikováno v:
Het pediatrisch formularium; een praktische leidraad, 87-97
STARTPAGE=87;ENDPAGE=97;TITLE=Het pediatrisch formularium; een praktische leidraad
STARTPAGE=87;ENDPAGE=97;TITLE=Het pediatrisch formularium; een praktische leidraad
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=narcis______::cca427bb9aa57d53275359a5fdf291a1
https://pure.eur.nl/en/publications/c28e0462-e78d-4458-9c6e-e00b05cec820
https://pure.eur.nl/en/publications/c28e0462-e78d-4458-9c6e-e00b05cec820
Autor:
Louise C. Wilson, Susan Tomkins, Richard J. Cornall, Wilkie Aom., Sally Ann Lynch, Vikram P Sharma, O Jeelani, Peter Donnelly, Steven A. Wall, David Johnson, Julie M. Phipps, Sophia C. Bennett, Alexander Kanapin, John B. Mulliken, Hoogeboom Ajm., P.J. van der Spek, Goos Jac., Elizabeth Sweeney, Simon J. McGowan, Angela F. Brady, Mathijssen Imj., Aimee L. Fenwick, Dylan J. Murray, John Broxholme, Robert E. Maxson, Twigg Srf., M S Brockop
Publikováno v:
The Lancet. 381:S114
Background Craniosynostosis, the premature fusion of the cranial sutures, is the second most common craniofacial malformation. A genetic aetiology can be identified in about 21% of cases, including mutations of TWIST1 that cause Saethre-Chotzen syndr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1d89ae9b1ed09f5eb913229a132e92dc
https://doi.org/10.1016/s0140-6736(13)60554-1
https://doi.org/10.1016/s0140-6736(13)60554-1