Phenotypic analysis of triphalangeal thumb and associated hand malformations.

অনুযায়ী Zguricas, J, Snijders, P J, Hovius, S E, Heutink, P, Oostra, B A, Lindhout, D
প্রকাশিত 1994

N-acetyltransferase-2 polymorphism in Parkinson's disease: the Rotterdam study

অনুযায়ী Harhangi, B, Oostra, B., Heutink, P., van Duijn, C. M, Hofman, A., Breteler, M.
প্রকাশিত 1999

Tau Pathology in Two Dutch Families with Mutations in the Microtubule-Binding Region of Tau

অনুযায়ী Spillantini, M.G., Crowther, R.A., Kamphorst, W., Heutink, P., van Swieten, J.C.
প্রকাশিত 1998

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

অনুযায়ী Mostert, A., Jansen, B., Dijkstra, P., Wesby-van Swaay, E., van Horn, J., Heutink, P., Lindhout, D.
প্রকাশিত 2002

Apolipoprotein E4 in the temporal variant of frontotemporal dementia

অনুযায়ী Rosso, S, van Swieten, J C, Roks, G, van Duijn, C M, Heutink, P, Cruts, M, van Broeckhoven, C
প্রকাশিত 2002

Linkage of hereditary haemorrhagic telangiectasia to chromosome 9q34 and evidence for locus heterogeneity.

অনুযায়ী Heutink, P, Haitjema, T, Breedveld, G J, Janssen, B, Sandkuijl, L A, Bontekoe, C J, Westerman, C J, Oostra, B A
প্রকাশিত 1994

Linkage studies on Gilles de la Tourette syndrome: what is the strategy of choice?

অনুযায়ী Heutink, P, van de Wetering, B J, Pakstis, A J, Kurlan, R, Sandor, P, Oostra, B A, Sandkuijl, L A
প্রকাশিত 1995

A new polymorphic probe on chromosome 22: NB17 (D22S181)

অনুযায়ী Deprez, R.H.Lekanne, Van Biezen, N.A., Heutink, P., Boejharat, K.R.G.S., De Klein, A., Van Kessel, A.H.M.Geurts, Zwarthoff, E.C.
প্রকাশিত 1991

A new polymorphic probe on chromosome 22: NB35 (D22S182)

অনুযায়ী Deprez, R.H.Lekanne, Van Biezen, N.A., Heutink, P., Boejharat, K.R.G.S., De Klein, A., Van Kessel, A.H.M.Geurts, Zwarthoff, E.C.
প্রকাশিত 1991

A new polymorphic probe on chromosome 22: NB84 (D22S183)

অনুযায়ী Deprez, R.H.Lekanne, van Biezen, N.A., Heutink, P., Boejharat, K.R.G.S., de Klein, A., van Kessel, A.H.M.Geurts, Zwarthoff, E.C.
প্রকাশিত 1991

A new polymorphic probe on chromosome 22q: NB129 (D22S193)

অনুযায়ী Deprez, R.H.Lekanne, Van Biezen, N.A., Heutink, P., Boejharat, K.R.G.S., De Klein, A., Van Kessel, A.H.M.Geurts, Zwarthoff, E.C.
প্রকাশিত 1991

No evidence for genetic linkage of Gilles de la Tourette syndrome on chromosomes 7 and 18.

অনুযায়ী Heutink, P, van de Wetering, B J, Breedveld, G J, Weber, J, Sandkuyl, L A, Devor, E J, Heiberg, A, Niermeijer, M F, Oostra, B A
প্রকাশিত 1990

Clinical and genetic studies on 12 preaxial polydactyly families and refinement of the localisation of the gene responsible to a 1.9 cM region on chromosome 7q36

অনুযায়ী Zguricas, J., Heus, H., Morales-Peralta, E., Breedveld, G., Kuyt, B., Mumcu, E., Bakker, W., Akarsu, N., Kay, S., Hovius, S., Heredero-Baute, L., Oostra, B., Heutink, P.
প্রকাশিত 1999

Novel mutations in three families confirm a major role of COL4A1 in hereditary porencephaly

অনুযায়ী Breedveld, G, de Coo, I F, Lequin, M H, Arts, W F M, Heutink, P, Gould, D B, John, S W M, Oostra, B, Mancini, G M S
প্রকাশিত 2006

Loss of function of DJ-1 triggered by Parkinson’s disease-associated mutation is due to proteolytic resistance to caspase-6

অনুযায়ী Giaime, E., Sunyach, C., Druon, C., Scarzello, S., Robert, G., Grosso, S., Auberger, P., Goldberg, M.S., Shen, J., Heutink, P., Pouysségur, J., Pagès, G., Checler, F., Costa, Alves da
প্রকাশিত 2010

A novel susceptibility locus for Hirschsprung's disease maps to 4q31.3–q32.3

অনুযায়ী Brooks, A S, Leegwater, P A, Burzynski, G M, Willems, P J, de Graaf, B, van Langen, I, Heutink, P, Oostra, B A, Hofstra, R M W, Bertoli‐Avella, A M
প্রকাশিত 2006

Acheiropodia Is Caused by a Genomic Deletion in C7orf2, the Human Orthologue of the Lmbr1 Gene

অনুযায়ী Ianakiev, P., van Baren, M. J., Daly, M. J., Toledo, S. P. A., Cavalcanti, M. G., Neto, J. Correa, Silveira, E. Lemos, Freire-Maia, A., Heutink, P., Kilpatrick, M. W., Tsipouras, P.
প্রকাশিত 2001

High prevalence of mutations in the microtubule-associated protein tau in a population study of frontotemporal dementia in the Netherlands.

অনুযায়ী Rizzu, P, Van Swieten, J C, Joosse, M, Hasegawa, M, Stevens, M, Tibben, A, Niermeijer, M F, Hillebrand, M, Ravid, R, Oostra, B A, Goedert, M, van Duijn, C M, Heutink, P
প্রকাশিত 1999

PARK7, a Novel Locus for Autosomal Recessive Early-Onset Parkinsonism, on Chromosome 1p36

অনুযায়ী van Duijn, C. M., Dekker, M. C. J., Bonifati, V., Galjaard, R. J., Houwing-Duistermaat, J. J., Snijders, P. J. L. M., Testers, L., Breedveld, G. J., Horstink, M., Sandkuijl, L. A., van Swieten, J. C., Oostra, B. A., Heutink, P.
প্রকাশিত 2001

Determining the genome-wide kinship coefficient seems unhelpful in distinguishing consanguineous couples with a high versus low risk for adverse reproductive outcome

অনুযায়ী Kelmemi, W., Teeuw, M. E., Bochdanovits, Z., Ouburg, S., Jonker, M. A., Alkuraya, F., Hashem, M., Kayserili, H., van Haeringen, A., Sheridan, E., Masri, A., Cobben, J. M., Rizzu, P., Kostense, P. J., Dommering, C. J., Henneman, L., Bouhamed-Chaabouni, H., Heutink, P., ten Kate, L. P., Cornel, M. C.
প্রকাশিত BMC Med Genet (2015)