Zobrazeno 1 - 10
of 991
pro vyhledávání: '"Fryns, J.P."'
Autor:
Isrie, M., Froyen, G., Devriendt, K., de Ravel, T., Fryns, J.P., Vermeesch, J.R., Van Esch, H.
Publikováno v:
In European Journal of Medical Genetics November 2012 55(11):577-585
Publikováno v:
In Neuropsychologia 2007 45(5):885-895
Autor:
Van Buggenhout, G.J.C.M. *, van Ravenswaaij-Arts, C., Mieloo, H., Syrrou, M., Hamel, B., Brunner, H., Fryns, J.P.
Publikováno v:
In Annales de genetique 2001 44(2):89-92
Autor:
van den Borne, H.W., van Hooren, R.H., van Gestel, M., Rienmeijer, P., Fryns, J.P., Curfs, L.M.G. *
Publikováno v:
In Patient Education and Counseling 1999 38(3):205-216
Autor:
Witters, G., Van Robays, J., Willekes, C., Coumans, A., Peeters, H., Gyselaers, W., Fryns, J.P.
Publikováno v:
Facts, Views & Vision in ObGyn
First trimester spontaneous abortions occur in 15 to 20% of all clinically recognized pregnancies. Chromosomal -anomalies are responsible for more than 50% of spontaneous abortions. The majority (90%) of these chromosomal anomalies are numerical, par
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a18405b8e18db9c227980d7a945a39c1
http://europepmc.org/articles/PMC3991414
http://europepmc.org/articles/PMC3991414
Velo-cardio-facial syndrome: guidelines for diagnosis, treatment and follow-up of ent manifestations
Publikováno v:
Acta Oto-Rhino-Laryngologica Belgica, 57, 2, pp. 101-6
Acta Oto-Rhino-Laryngologica Belgica, 57, 101-6
Acta Oto-Rhino-Laryngologica Belgica, 57, 101-6
Item does not contain fulltext The Velo-Cardio-Facial Syndrome (VCFS), caused by a submicroscopic deletion in the long arm of chromosome 22, has a broad clinical spectrum of ENT manifestations including for instance velopharyngeal dysfunction, hearin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::bb45e4e3b0cd66f5cf84691ff6577e44
https://hdl.handle.net/2066/144259
https://hdl.handle.net/2066/144259
Publikováno v:
Genetic Counseling, 10, 59-65
Genetic Counseling, 10, pp. 59-65
Genetic Counseling, 10, pp. 59-65
Item does not contain fulltext
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::dc7d4126cf39cb20f42db8720dde6f06
https://hdl.handle.net/2066/186156
https://hdl.handle.net/2066/186156
Publikováno v:
Genetic Counseling, 9, 3, pp. 201-204
Genetic Counseling, 9, 201-204
Genetic Counseling, 9, 201-204
Item does not contain fulltext 4 p.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::d0df6b94d9f9cb59b86db481b205771c
https://hdl.handle.net/2066/166802
https://hdl.handle.net/2066/166802
Publikováno v:
Nederlands Tijdschrift voor Geneeskunde, 53, pp. 1506-1513
Nederlands Tijdschrift voor Geneeskunde
Nederlands Tijdschrift voor Geneeskunde, 1506-1513
STARTPAGE=1506;ENDPAGE=1513;ISSN=0028-2162;TITLE=Nederlands Tijdschrift voor Geneeskunde
Nederlands Tijdschrift voor Geneeskunde
Nederlands Tijdschrift voor Geneeskunde, 1506-1513
STARTPAGE=1506;ENDPAGE=1513;ISSN=0028-2162;TITLE=Nederlands Tijdschrift voor Geneeskunde
Item does not contain fulltext
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::1b257977b43a60e517c27bf02c0bccd9
https://hdl.handle.net/2066/164172
https://hdl.handle.net/2066/164172
Autor:
Renard, M., Callewaert, B, Baetens, Machteld, Fryns, J.p., Bonduelle, Mary-Louise, Coucke, Paul, Loeys, B., De Paepe, A., De Backer, J.
BACKGROUND: Thoracic aortic aneurysm/dissection (TAAD) is a common phenotype that may occur as an isolated manifestation or within the constellation of a defined syndrome. In contrast to syndromic TAAD, the elucidation of the genetic basis of isolate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3848::1ad29d96a01addfa8aaa013bae074db6
https://hdl.handle.net/20.500.14017/0b192e94-f7d2-4046-90ce-c229811132ea
https://hdl.handle.net/20.500.14017/0b192e94-f7d2-4046-90ce-c229811132ea
