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

由 Mariman, E C, Hamel, B C
出版 1992

The p63 gene in EEC and other syndromes

由 Brunner, H, Hamel, B, van Bokhoven, H
出版 2002

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

由 Copeland, J. A., Hamel, B., Bourne, J. R.
出版 1979

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

由 Rump, R, Hamel, B C, Pinckers, A J, van Dop, P A
出版 1997

Intestinal pseudo-obstruction in myotonic dystrophy.

由 Brunner, H G, Hamel, B C, Rieu, P, Höweler, C J, Peters, F T
出版 1992

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

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

Down-Turner syndrome: case report and review.

由 Van Buggenhout, G J, Hamel, B C, Trommelen, J C, Mieloo, H, Smeets, D F
出版 1994

Marfan syndrome masked by Down syndrome?

由 Vis, J.C., van Engelen, K., Timmermans, J., Hamel, B.C., Mulder, B.J.M.
出版 2009

Oculocerebrocutaneous syndrome.

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

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

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

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

由 Ali, A. M., Mbwasi, R. M., Kinabo, G., Kamsteeg, E.-J., Hamel, B. C., Dekker, M. C. J.
發表在 Case Rep Genet (2017)

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

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

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

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

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

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

Adult Phenotypes in Angelman- and Rett-Like Syndromes

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

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

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

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

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

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

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

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

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

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