Zobrazeno 1 - 10
of 168
pro vyhledávání: '"Went, L N"'
Autor:
de Vries-de Mol, E.C., Went, L. N.
Publikováno v:
Human Heredity, 1978 Jan 01. 28(4), 301-316.
Externí odkaz:
https://www.jstor.org/stable/45100642
Autor:
MacIver, J. E., Went, L. N.
Publikováno v:
The British Medical Journal, 1960 Mar 01. 1(5175), 775-779.
Externí odkaz:
https://www.jstor.org/stable/25390584
Autor:
Went, L. N., MacIver, J. E.
Publikováno v:
The British Medical Journal, 1959 Aug 01. 2(5144), 138-139.
Externí odkaz:
https://www.jstor.org/stable/25388106
Autor:
de Jong, W. W. W., Went, L. N.
Publikováno v:
Acta Genetica et Statistica Medica, 1968 Jan 01. 18(5), 429-443.
Externí odkaz:
https://www.jstor.org/stable/45104144
Autor:
WENT, L. N.
Publikováno v:
Acta Genetica et Statistica Medica, 1964 Jan 01. 14(3/4), 220-239.
Externí odkaz:
https://www.jstor.org/stable/45103641
Autor:
de Jong, W. W., Went, L. N.
Publikováno v:
Human Heredity, 1974 Jan 01. 24(1), 32-39.
Externí odkaz:
https://www.jstor.org/stable/45101063
Autor:
Fraser, G. R., Volkers, W. S., Bernini, L. F., de Greve, W. B., van Loghem, E., Khan, P. Meera, Nijenhuis, L. E., Veltkamp, J. J., Vogel, G. P., Went, L. N.
Publikováno v:
Human Heredity, 1974 Jan 01. 24(5/6), 424-434.
Externí odkaz:
https://www.jstor.org/stable/45101108
Autor:
Vries, D. D., Went, L. N., Bruyn, G. W., Scholte, H. R., Robert Hofstra, Bolhuis, P. A., Oost, B. A.
Publikováno v:
American Journal of Human Genetics, 58(4), 703-711. CELL PRESS
Scopus-Elsevier
Scopus-Elsevier
A rare form of Leber hereditary optic neuropathy (LHON) that is associated with hereditary spastic dystonia has been studied in a large Dutch family. Neuropathy and ophthalmological lesions were present together in some family members, whereas only o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::ff5f15cd9b5a127ca4bc64c82e30057d
https://europepmc.org/articles/PMC1914692/
https://europepmc.org/articles/PMC1914692/
Tritanopia is an autosomal dominant genetic disorder of human vision characterize by a selective deficiency of blue spectral sensitivity. The defect is manifested within the retina and could be caused by a deficiency in function or numbers (or both)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::71fbf1ecf6a9b5bb47203dc299ccd4a7
https://europepmc.org/articles/PMC1684278/
https://europepmc.org/articles/PMC1684278/
Autor:
Went, L. N.
Publikováno v:
Cytogenetics & Cell Genetics; Aug99, Vol. 86 Issue 2, p153-156, 4p