Zobrazeno 1 - 6
of 6
pro vyhledávání: '"G. J. Te Meerman"'
Autor:
Joep H. A. M. Tuerlings, Maaike W. G. Looman, Jan A.M. Kremer, Hans Scheffer, Eric J.H. Meuleman, Ben W.J. Mol, H. M. W. M. Merkus, Charles H.C.M. Buys, G. J. Te Meerman
Publikováno v:
Fertility and sterility. 69(5)
OBJECTIVE: To examine the frequency of anomalies of the vas deferens and the frequency of mutations of the cystic fibrosis transmembrane regulator (CFTR) gene in male candidates for intracytoplasmic sperm injection (ICSI) who had severe oligoasthenot
Autor:
G. J. Te Meerman, M. A. Van Der Meulen, Charles H.C.M. Buys, H. de Vries, Hans Scheffer, L.P. ten Kate, Dicky J. J. Halley, R. Rozen
Publikováno v:
HUMAN GENETICS, 98(3), 304-309. SPRINGER
HUMAN GENETICS, 98(3), 304-9. SPRINGER
HUMAN GENETICS, 98(3), 304-9. SPRINGER
Cystic fibrosis (CF) patients with the A455E mutation, in both the French Canadian and the Dutch population, share a common haplotype over distances of up to 25 cM. French Canadian patients with the 621+1G-->T mutation share a common haplotype of mor
Autor:
J E Dankert-Roelse, G J te Meerman
Publikováno v:
Thorax, 50(7), 712-8. BMJ PUBLISHING GROUP
BACKGROUND--A study was undertaken to evaluate whether an early diagnosis by neonatal screening may improve the long term prognosis of patients with cystic fibrosis and to assess the influence of expert management started immediately after the diagno
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4c81829a345ea704a68b17d866a38ee3
https://research.rug.nl/en/publications/eaf6de0a-adff-4df2-937e-dcf3713f810f
https://research.rug.nl/en/publications/eaf6de0a-adff-4df2-937e-dcf3713f810f
Autor:
G J, te Meerman, J E, Dankert-Roelse
Publikováno v:
Advances in experimental medicine and biology. 290
Publikováno v:
Lancet, 1(8484), 802-803. Elsevier Limited
LANCET, 1(8484), 802-803. ELSEVIER SCIENCE INC
Dankert-Roelse, J E, Meerman, G J, Cornel, M C, Knol, K & ten Kate, L P 1986, ' Neonatal screening for cystic fibrosis ', Lancet, vol. 1, no. 8484, pp. 802-803 . https://doi.org/10.1016/0009-8981(81)90145-5
Dankert-Roelse, J E, Te Meerman, G J, Cornel, M C, Knol, K & Ten Kate, L P 1986, ' NEONATAL SCREENING FOR CYSTIC FIBROSIS ', The Lancet, vol. 327, no. 8484, pp. 802-803 . https://doi.org/10.1016/S0140-6736(86)91812-X
The Lancet, 327(8484), 802-803. Elsevier Limited
LANCET, 1(8484), 802-803. ELSEVIER SCIENCE INC
Dankert-Roelse, J E, Meerman, G J, Cornel, M C, Knol, K & ten Kate, L P 1986, ' Neonatal screening for cystic fibrosis ', Lancet, vol. 1, no. 8484, pp. 802-803 . https://doi.org/10.1016/0009-8981(81)90145-5
Dankert-Roelse, J E, Te Meerman, G J, Cornel, M C, Knol, K & Ten Kate, L P 1986, ' NEONATAL SCREENING FOR CYSTIC FIBROSIS ', The Lancet, vol. 327, no. 8484, pp. 802-803 . https://doi.org/10.1016/S0140-6736(86)91812-X
The Lancet, 327(8484), 802-803. Elsevier Limited
Autor:
R Williamson, Charles H.C.M. Buys, G. J. Te Meerman, L.P. ten Kate, I. Dijkstra, D. Penninga, M Farrall
Publikováno v:
Pediatric Research. 20:1044-1044
Several groups recently reported DNA markers on chromosome 7 in linkage with the locus of the cystic fibrosis (CF) mutation. From the linkage data collected to date probes pJ3.11 and met appear to be sufficiently close to the CF locus (each with abou