Zobrazeno 1 - 10
of 94
pro vyhledávání: '"Delleman, J. W."'
Publikováno v:
Clinical genetics, 45(5), 236-240. Wiley-Blackwell
X-linked progressive cone dystrophy (XLPCD) is characterized by progressive macular atrophy, abnormal colour vision, reduced cone responses in ERG, and reduced visual acuity. XLPCD may be genetically heterogeneous. Therefore, carrier detections by DN
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=narcis______::ded3e70c1ff4a86a3a32590172c88845
https://pure.amc.nl/en/publications/dna-carrier-detection-in-xlinked-progressive-cone-dystrophy(c67c844f-70db-4aac-a712-5289285a0766).html
https://pure.amc.nl/en/publications/dna-carrier-detection-in-xlinked-progressive-cone-dystrophy(c67c844f-70db-4aac-a712-5289285a0766).html
Publikováno v:
Neuropediatrics; 1998, Vol. 29 Issue 6, p294-297, 4p
Publikováno v:
Neurology; Jun1978, Vol. 28 Issue 6, p567-570, 4p
Autor:
de JONG, J. G.Y., DELLEMAN, J. W., HOUBEN, M., MANSCHOT, W. A., de MINJER, A., MOL, J., SLOOFF, J. L.
Publikováno v:
Neurology; Dec1976, Vol. 26 Issue 12, p1152-1158, 7p
Autor:
Dorp, D. B. van, Eriksson, A. W., Delleman, J. W., Vliet, A. G. M. van, Collewijn, H., Balen, A. Th. M. van, Forsius, H. R.
Publikováno v:
Clinical Genetics; Dec1985, Vol. 28 Issue 6, p526-531, 6p
Publikováno v:
Clinical Genetics; Nov1984, Vol. 26 Issue 5, p440-444, 5p
Autor:
Delleman, J. W., Oorthuys, J. W. E.
Publikováno v:
Clinical Genetics; Mar1981, Vol. 19 Issue 3, p191-198, 8p
Autor:
Delleman, J W, de Jong, P T
Publikováno v:
British Journal of Ophthalmology; Oct1985, Vol. 69 Issue 10, p754-757, 4p, 3 Black and White Photographs, 1 Diagram
Autor:
Meire, F. M., Delleman, J. W.
Publikováno v:
Ophthalmic Paediatrics & Genetics; 1992, Vol. 13 Issue 2, p123-129, 7p
Publikováno v:
Ophthalmic Paediatrics & Genetics; 1991, Vol. 12 Issue 3, p153-157, 5p