Zobrazeno 1 - 10
of 2 201
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
Autor:
Abiad, May1 (AUTHOR), Zargarzadeh, Nikan1 (AUTHOR), Javinani, Ali1 (AUTHOR), Krispin, Eyal1 (AUTHOR), Shamshirsaz, Alireza A.1 (AUTHOR) alireza.shamshirsaz@childrens.harvard.edu
Publikováno v:
Journal of Clinical Medicine. Oct2024, Vol. 13 Issue 20, p6245. 15p.
Autor:
Woolley, Shernae A.1 (AUTHOR), Hopkins, Bethany1 (AUTHOR), Khatkar, Mehar S.1 (AUTHOR), Jerrett, Ian V.2 (AUTHOR), Willet, Cali E.3 (AUTHOR), O'Rourke, Brendon A.4 (AUTHOR) brendon.orourke@dpi.nsw.gov.au, Tammen, Imke1 (AUTHOR) imke.tammen@sydney.edu.au
Publikováno v:
Animals (2076-2615). Oct2024, Vol. 14 Issue 19, p2811. 18p.
Autor:
Tangshewinsirikul, Chayada1 (AUTHOR), Wattanasirichaigoon, Duangrurdee2 (AUTHOR) duangrurdee.wat@mahidol.ac.th, Tim-Aroon, Thipwimol2 (AUTHOR), Promsonthi, Patama1 (AUTHOR), Katanyuwong, Poomiporn2 (AUTHOR), Diawtipsukon, Sanpon1 (AUTHOR), Chansriniyom, Nareenun1 (AUTHOR), Tongsong, Theera3 (AUTHOR) duangrurdee.wat@mahidol.ac.th
Publikováno v:
Journal of Clinical Medicine. Oct2024, Vol. 13 Issue 19, p5735. 12p.
Autor:
Haidurov, Alexander1 (AUTHOR) haiduroa@tcd.ie, Budanov, Andrei V.1 (AUTHOR) haiduroa@tcd.ie
Publikováno v:
Cells (2073-4409). Sep2024, Vol. 13 Issue 18, p1587. 19p.
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