Tagariello, A., Heller, R., Greven, A., Kalscheuer, Vera M., Molter, T., Rauch, A., ...
Craniosynostosis is a congenital developmental disorder involving premature fusion of cranial sutures, which results in an abnormal shape of the skull. Significant progress in understanding the...
Loeys, B, Chen, J, Neptune, E, Judge, D, Podowski, M, Holm, T, ...
We report heterozygous mutations in the genes encoding either type I or type II transforming growth factor beta receptor in ten families with a newly described human phenotype that includes...
Twenty-six novel EFNB1 mutations in familial and sporadic craniofrontonasal syndrome (CFNS) (2005)
Wieland, I., Reardon, W., Jakubiczka, S., Franco, B., Kress, W., Vincent-Delorme, C., ...
Twenty-six novel EFNB1 mutations in familial and sporadic cranlofrontonasal syndrome (CFNS) (2005)
Wieland, I., Reardon, W., Jakubiczka, S., Franco, B., Kress, W., Vincent-Delorme, C., ...
Craniofrontonasal syndrome (CFNS) is an X-linked disorder characterized by a more severe manifestation in heterozygous females than in hemizygous males. Heterozygous females have craniofrontonasal...
Twenty-six novel EFNB1 mutations in familial and sporadic cranlofrontonasal syndrome (CFNS) (2005)
Wieland, I., Reardon, W., Jakubiczka, S., Franco, B., Kress, W., Vincent-Delorme, C., ...
Craniofrontonasal syndrome (CFNS) is an X-linked disorder characterized by a more severe manifestation in heterozygous females than in hemizygous males. Heterozygous females have craniofrontonasal...
Twenty-six novel EFNB1 mutations in familial and sporadic craniofrontonasal syndrome (CFNS) (2005)
Wieland, I., Reardon, W., Jakubiczka, S., Franco, B., Kress, W., Vincent-Delorme, C., ...
Schneider, C, Gil, FP, Schneider, M, Anetseder, M, Kress, W, Müller, CR
We report a patient with proximal myotonic myopathy who was treated with neuroleptics because of exacerbating schizophrenia. Under therapy with fluanxol, the patient developed muscle stiffness and...
Surface lattice dynamics of Mg(0001) (2000)
Ismail, P., Hofmann, E., Plummer, W., Bungaro, C., Kress, W.
Mutations in the MTM1 gene implicated in X-linked myotubular myopathy (1997)
Laporte, J., Guiraud-Chaumeil, C., Vincent, M.C., Mandel, J.L., Tanner, S.M., Liechti-Gallati, S., ...
LATTICE DYNAMICS OF CUPRITE (Cu2O) (1981)
Kugel, G., Carabatos, C., Kress, W.
The phonon dispersion curves of Cu2O have been calculated using a shell model which takes into account nearest neighbour O-Cu, Cu-Cu and O-O interactions, long range Coulomb interactions and the...
PHONONS IN MIXED VALENCE COMPOUNDS (1981)
Kress, W., Bilz, H., Güntherodt, G., Jayaraman, A.
Several mixed-valence NaCl-structure compounds show strong anomalies in the phonon dispersion curves. These anomalies are related to the interaction of localized f-electrons with delocalized band...
LATTICE DYNAMICS OF CUPRITE (Cu2O) (1981)
Kugel, G., Carabatos, C., Kress, W.
The phonon dispersion curves of Cu2O have been calculated using a shell model which takes into account nearest neighbour O-Cu, Cu-Cu and O-O interactions, long range Coulomb interactions and the...
PHONONS IN MIXED VALENCE COMPOUNDS (1981)
Kress, W., Bilz, H., Güntherodt, G., Jayaraman, A.
Several mixed-valence NaCl-structure compounds show strong anomalies in the phonon dispersion curves. These anomalies are related to the interaction of localized f-electrons with delocalized band...
LATTICE DYNAMICS OF CUPRITE (Cu2O) (1981)
Kugel, G., Carabatos, C., Kress, W.
The phonon dispersion curves of Cu2O have been calculated using a shell model which takes into account nearest neighbour O-Cu, Cu-Cu and O-O interactions, long range Coulomb interactions and the...
PHONONS IN MIXED VALENCE COMPOUNDS (1981)
Kress, W., Bilz, H., Güntherodt, G., Jayaraman, A.
Several mixed-valence NaCl-structure compounds show strong anomalies in the phonon dispersion curves. These anomalies are related to the interaction of localized f-electrons with delocalized band...
Linkage studies in a large fragile X family.
Patterson, M, Bell, M, Kress, W, Davies, K E, Froster-Iskenius, U
We have analyzed the segregation of five loci in the region Xq27/28 in a large family affected by the fragile X syndrome. The marker DXS115 (767) is shown to be polymorphic with the enzyme PstI, as...
Felbor, U., Mutsch, Y., Grehn, F., Muller, C., Kress, W.
AIMS—To assess the involvement of the recently identified human homogentisate 1,2-dioxygenase gene (HGO) in alkaptonuria (AKU) in two unrelated patients with ochronosis of the conjunctiva, sclera,...
No evidence for heterogeneity in oculopharyngeal muscular dystrophy.
Kress, W, Halliger-Keller, B, Grimm, T, Porschke, H, Engelhardt, A, Goebel, H H, ...
Merienne, K, Jacquot, S, Trivier, E, Pannetier, S, Rossi, A, Scott, C, ...
Coffin-Lowry syndrome (CLS) is a syndromal form of X linked mental retardation, in which some associated facial, hand, and skeletal abnormalities are diagnostic features. Accurate diagnosis, critical...