Neonatal form of dystrophia myotonica. Five cases in preterm babies and a review of earlier reports.

nork Pearse, R G, Höweler, C J
Argitaratua 1979

Intestinal pseudo-obstruction in myotonic dystrophy.

nork Brunner, H G, Hamel, B C, Rieu, P, Höweler, C J, Peters, F T
Argitaratua 1992

MASA syndrome (a form of complicated spastic paraplegia) and X linked hydrocephalus: variable expression of the same mutation at Xq28? Call for families.

nork Schrander-Stumpel, C, Fryns, J, Cassiman, J J, Legius, E, Spaepen, A, Höweler, C J
Argitaratua 1992

Arthrogryposis, ophthalmoplegia, and retinopathy: confirmation of a new type of arthrogryposis.

nork Schrander-Stumpel, C T, Höweler, C J, Reekers, A D, De Smet, N M, Hall, J G, Fryns, J P
Argitaratua 1993

Paternal transmission of congenital myotonic dystrophy.

nork de Die-Smulders, C E, Smeets, H J, Loots, W, Anten, H B, Mirandolle, J F, Geraedts, J P, Höweler, C J
Argitaratua 1997

Anticipation resulting in elimination of the myotonic dystrophy gene: a follow up study of one extended family.

nork de Die-Smulders, C E, Höweler, C J, Mirandolle, J F, Brunner, H G, Hovers, V, Brüggenwirth, H, Smeets, H J, Geraedts, J P
Argitaratua 1994

Influence of sex of the transmitting parent as well as of parental allele site on the CTG expansion in myotonic dystrophy (DM)

nork Brunner, H. G., Brüggenwirth, H. T., Nillesen, W., Jansen, G., Hamel, B. C. J., Hoppe, R. L. E., de Die, C. E. M., Höweler, C. J., van Oost, B. A., Wieringa, B., Ropers, H. H., Smeets, H. J. M.
Argitaratua 1993