Charcot-Marie-Tooth disease.

Por Heimans, J J, Lindhout, D
Publicado em 1983

Concordant cerebral oligodendroglioma in identical twins.

Por Roelvink, N C, Kamphorst, W, Lindhout, D, Ponssen, H
Publicado em 1986

Phenotypic analysis of triphalangeal thumb and associated hand malformations.

Por Zguricas, J, Snijders, P J, Hovius, S E, Heutink, P, Oostra, B A, Lindhout, D
Publicado em 1994

Bilateral hereditary micro-epiphyseal dysplasia: Further delineation of the phenotype with 40 years follow-up

Por Mostert, A., Jansen, B., Dijkstra, P., Wesby-van Swaay, E., van Horn, J., Heutink, P., Lindhout, D.
Publicado em 2002

Mutations in mitochondrial tRNA genes: non-linkage with syndromes of Wolfram and chronic progressive external ophthalmoplegia.

Por van den Ouweland, J M, Bruining, G J, Lindhout, D, Wit, J M, Veldhuyzen, B F, Maassen, J A
Publicado em 1992

Metacarpophalangeal pattern (MCPP) profile analysis in a family with triphalangeal thumb.

Por Zguricas, J, Dijkstra, P F, Gelsema, E S, Snijders, P J, Wüstefeld, H P, Venema, H W, Hovius, S E, Lindhout, D
Publicado em 1997

Silver-Russell phenotype in a patient with pure trisomy 1q32.1-q42.1: further delineation of the pure 1q trisomy syndrome

Por van Haelst, M M, Eussen, H, Visscher, F, de Ruijter, J L M, Drop, S, Lindhout, D, Wouters, C, Govaerts, L
Publicado em 2002

A leucine-to-proline mutation in the insulin receptor in a family with insulin resistance.

Por Klinkhamer, M P, Groen, N A, van der Zon, G C, Lindhout, D, Sandkuyl, L A, Krans, H M, Möller, W, Maassen, J A
Publicado em 1989

Mutational spectrum of the TSC1 gene in a cohort of 225 tuberous sclerosis complex patients: no evidence for genotype-phenotype correlation

Por van Slegtenhorst, M., Verhoef, S., Tempelaars, A., Bakker, L., Wang, Q., Wessels, M., Bakker, R., Nellist, M., Lindhout, D., Halley, D., van den Ouweland, A.
Publicado em 1999

Genotype‐phenotype relationship in hereditary haemorrhagic telangiectasia

Por Letteboer, T G W, Mager, J J, Snijder, R J, Koeleman, B P C, Lindhout, D, van Amstel, J K Ploos, Westermann, C J J
Publicado em 2006

Familial cylindromatosis mimicking tuberous sclerosis complex and confirmation of the cylindromatosis locus, CYLD1, in a large family.

Por Verhoef, S, Schrander-Stumpel, C T, Vuzevski, V D, Tempelaars, A, Jansen, L A, Malfeyt, G A, Ceelen, T L, Lindhout, D, Halley, D J, van den Ouweland, A M
Publicado em 1998

Linkage to markers for the chromosome region 17q12-q21 in 13 Dutch breast cancer kindreds

Por Devilee, P., Cornelis, R. S., Bootsma, A., Bardoel, A., van Vliet, M., van Leeuwen, I., Cletor, F. J., de Klein, A., Lindhout, D., Vasen, H. F. A., Cornelisse, C. J., Khan, P. Meera
Publicado em 1993

High rate of mosaicism in tuberous sclerosis complex.

Por Verhoef, S, Bakker, L, Tempelaars, A M, Hesseling-Janssen, A L, Mazurczak, T, Jozwiak, S, Fois, A, Bartalini, G, Zonnenberg, B A, van Essen, A J, Lindhout, D, Halley, D J, van den Ouweland, A M
Publicado em 1999

Identification of a nonsense mutation at the 5' end of the TSC2 gene in a family with a presumptive diagnosis of tuberous sclerosis complex.

Por Vrtel, R, Verhoef, S, Bouman, K, Maheshwar, M M, Nellist, M, van Essen, A J, Bakker, P L, Hermans, C J, Bink-Boelkens, M T, van Elburg, R M, Hoff, M, Lindhout, D, Sampson, J, Halley, D J, van den Ouweland, A M
Publicado em 1996

Atypical HNPCC owing to MSH6 germline mutations: analysis of a large Dutch pedigree

Por Wagner, A, Hendriks, Y, Meijers-Heijboer, E, de Leeuw, W J F, Morreau, H, Hofstra, R, Tops, C, Bik, E, Brocker-Vriends, A, van der Meer, C, Lindhout, D, Vasen, H, Breuning, M, Cornelisse, C, van Krimpen, C, Niermeijer, M, Zwinderman, A, Wijnen, J, Fodde, R
Publicado em 2001

Majority of hMLH1 mutations responsible for hereditary nonpolyposis colorectal cancer cluster at the exonic region 15-16.

Por Wijnen, J., Khan, P. M., Vasen, H., Menko, F., van der Klift, H., van den Broek, M., van Leeuwen-Cornelisse, I., Nagengast, F., Meijers-Heijboer, E. J., Lindhout, D., Griffioen, G., Cats, A., Kleibeuker, J., Varesco, L., Bertario, L., Bisgaard, M. L., Mohr, J., Kolodner, R., Fodde, R.
Publicado em 1996