Sex ratios of affected and transmitting members of multiple case families with neural tube defects.

od Mariman, E C, Hamel, B C
Izdano 1992

The p63 gene in EEC and other syndromes

od Brunner, H, Hamel, B, van Bokhoven, H
Izdano 2002

An Exploratory Data Analysis System for Support in Medical Decision-Making

od Copeland, J. A., Hamel, B., Bourne, J. R.
Izdano 1979

Two sibs with chorioretinal dystrophy, hypogonadotrophic hypogonadism, and cerebellar ataxia: Boucher-Neuhäuser syndrome.

od Rump, R, Hamel, B C, Pinckers, A J, van Dop, P A
Izdano 1997

Intestinal pseudo-obstruction in myotonic dystrophy.

od Brunner, H G, Hamel, B C, Rieu, P, Höweler, C J, Peters, F T
Izdano 1992

Molecular definition of the chromosome 7 deletion in Williams syndrome and parent-of-origin effects on growth.

od Pérez Jurado, L. A., Peoples, R., Kaplan, P., Hamel, B. C., Francke, U.
Izdano 1996

Down-Turner syndrome: case report and review.

od Van Buggenhout, G J, Hamel, B C, Trommelen, J C, Mieloo, H, Smeets, D F
Izdano 1994

Marfan syndrome masked by Down syndrome?

od Vis, J.C., van Engelen, K., Timmermans, J., Hamel, B.C., Mulder, B.J.M.
Izdano 2009

Oculocerebrocutaneous syndrome.

od Bleeker-Wagemakers, L M, Hamel, B C, Hennekam, R C, Beemer, F A, Oorthuys, H W
Izdano 1990

A new X linked neurodegenerative syndrome with mental retardation, blindness, convulsions, spasticity, mild hypomyelination, and early death maps to the pericentromeric region

od Hamel, B., Wesseling, P., Renier, W., van den Helm, B., Ropers, H., Kremer, H., Mariman, E.
Izdano 1999

Freeman–Sheldon Syndrome: First Molecularly Confirmed Case from Sub-Saharan Africa

od Ali, A. M., Mbwasi, R. M., Kinabo, G., Kamsteeg, E.-J., Hamel, B. C., Dekker, M. C. J.
Izdano u Case Rep Genet (2017)

A second gene for autosomal dominant Möbius syndrome is localized to chromosome 10q, in a Dutch family.

od Verzijl, H T, van den Helm, B, Veldman, B, Hamel, B C, Kuyt, L P, Padberg, G W, Kremer, H
Izdano 1999

Rare polymorphic variants of the AGTR2 gene in boys with non-specific mental retardation

od Bienvenu, T, Poirier, K, Van Esch, H, Hamel, B, Moraine, C, Fryns, J, Ropers, H, Beldjord, C, Yntema, H, Chelly, J
Izdano 2003

Jeune syndrome: description of 13 cases and a proposal for follow-up protocol

od de Vries, J., Yntema, J. L., van Die, C. E., Crama, N., Cornelissen, E. A. M., Hamel, B. C. J.
Izdano 2009

Adult Phenotypes in Angelman- and Rett-Like Syndromes

od Willemsen, M.H., Rensen, J.H.M., van Schrojenstein-Lantman de Valk, H.M.J., Hamel, B.C.J., Kleefstra, T.
Izdano 2012

A frameshift mutation in the gene for PAX3 in a girl with spina bifida and mild signs of Waardenburg syndrome.

od Hol, F A, Hamel, B C, Geurds, M P, Mullaart, R A, Barr, F G, Macina, R A, Mariman, E C
Izdano 1995

Xeroderma pigmentosum--Cockayne syndrome complex: a further case.

od Hamel, B C, Raams, A, Schuitema-Dijkstra, A R, Simons, P, van der Burgt, I, Jaspers, N G, Kleijer, W J
Izdano 1996

Genetic variation analysis of MLP, TFAP2A, and CSK in patients with neural tube defects

od Klootwijk, R, Hol, F, Wu, M, Willemen, J, Groenen, P, Hamel, B, Straatman, H, Steegers-Theuniss..., R, Mariman, E, Franke, B
Izdano 2003

The small patella syndrome: description of five cases from three families and examination of possible allelism with familial patella aplasia-hypoplasia and nail-patella syndrome

od BONGERS, E., VAN BOKHOVEN, H., VAN THIENEN, M.-N., KOOYMAN, M., VAN BEERSUM, S. E C, BOETES, C., KNOERS, N., HAMEL, B.
Izdano 2001

Contiguous gene syndromes due to deletions in the distal short arm of the human X chromosome.

od Ballabio, A, Bardoni, B, Carrozzo, R, Andria, G, Bick, D, Campbell, L, Hamel, B, Ferguson-Smith, M A, Gimelli, G, Fraccaro, M
Izdano 1989