Sickle-cell Anaemia Complicated by Megaloblastic Anaemia of Infancy

Por MacIver, J. E., Went, L. N.
Publicado em 1960

Sickle-Cell/Haemoglobin-J Disease

Por Went, L. N., MacIver, J. E.
Publicado em 1959

Linkage investigations in two families with hereditary ataxia.

Por Van Rossum, J, Veenema, H, Went, L N
Publicado em 1981

Primary choroidal and cutaneous melanomas, bilateral choroidal melanomas, and familial occurrence of melanomas.

Por Oosterhuis, J. A., Went, L. N., Lynch, H. T.
Publicado em 1982

Human tritanopia associated with a third amino acid substitution in the blue-sensitive visual pigment.

Por Weitz, C J, Went, L N, Nathans, J
Publicado em 1992

Haemoglobin Lepore Boston and elliptocytosis in a family of Indonesian-German ancestry.

Por Went, L N, de Jong, W W, Bos, S E
Publicado em 1975

Late onset dominant cone dystrophy with early blue cone involvement.

Por Went, L N, van Schooneveld, M J, Oosterhuis, J A
Publicado em 1992

Dominant cone dystrophy starting with blue cone involvement.

Por van Schooneveld, M J, Went, L N, Oosterhuis, J A
Publicado em 1991

Dominant cone dystrophy starting with blue cone involvement

Por Pinckers, A, Went, L N, Van Schooneveld, M J, Oosterhuis, J A
Publicado em 1992

A family with apparently sex-linked optic atrophy.

Por Went, L N, De Vries-De Mol, E C, Völker-Dieben, H J
Publicado em 1975

X linked progressive cone dystrophy with specific attention to carrier detection.

Por van Everdingen, J A, Went, L N, Keunen, J E, Oosterhuis, J A
Publicado em 1992

Human tritanopia associated with two amino acid substitutions in the blue-sensitive opsin.

Por Weitz, C J, Miyake, Y, Shinzato, K, Montag, E, Zrenner, E, Went, L N, Nathans, J
Publicado em 1992

Homozygous beta+ thalassaemia owing to a mutation in the cleavage-polyadenylation sequence of the human beta globin gene.

Por Losekoot, M, Fodde, R, Harteveld, C L, van Heeren, H, Giordano, P C, Went, L N, Bernini, L F
Publicado em 1991

Tumour spectrum in the FAMMM syndrome.

Por Lynch, H. T., Fusaro, R. M., Pester, J., Oosterhuis, J. A., Went, L. N., Rumke, P., Neering, H., Lynch, J. F.
Publicado em 1981

Genetic and biochemical impairment of mitochondrial complex I activity in a family with Leber hereditary optic neuropathy and hereditary spastic dystonia.

Por De Vries, D. D., Went, L. N., Bruyn, G. W., Scholte, H. R., Hofstra, R. M., Bolhuis, P. A., van Oost, B. A.
Publicado em 1996

Studies on African Pygmies. I. A pilot investigation of Babinga Pygmies in the Central African Republic (with an analysis of genetic distances).

Por Cavalli-Sforza, L L, Zonta, L A, Nuzzo, F, Bernini, L, de Jong, W W, Meera Khan, P, Ray, A K, Went, L N, Siniscalco, M, Nijenhuis, L E, van Loghem, E, Modiano, G
Publicado em 1969