Showing results (151-160 of 457) with videos related to
Sort By:
Pageof 46
Protein Science : a Publication of the Protein Society|March 27, 2004
Orientational potentials extracted from protein structures improve native fold recognitionNicolae-Viorel Buchete, John E Straub, Devarajan ThirumalaiProceedings of the National Academy of Sciences of the United States of America|October 7, 2004
Aqueous urea solution destabilizes Abeta(16-22) oligomersD K Klimov, John E Straub, D ThirumalaiEuropean Journal of Pediatrics|August 17, 1978
Mucopolysaccharidosis II (Hunter disease) with corneal opacities. Report on two patients at the extremes of a wide clinical spectrumJ Spranger, M Cantz, J Gehler, et al.Clinical Dysmorphology|January 11, 2001
Ischiospinal dysostosis with rib gaps and nephroblastomatosisJ Spranger, S Self, K B Clarkson, et al.American Journal of Medical Genetics. Part A|August 19, 2003
Congenital generalized lipodystrophy, mental retardation, deafness, short stature, and slender bones: a newly recognized syndrome?A Rajab, M Khaburi, S Spranger, et al.Pediatric Radiology|January 1, 1994
Kniest dysplasia is caused by dominant collagen II (COL2A1) mutations: parental somatic mosaicism manifesting as Stickler phenotype and mild spondyloepiphyseal dysplasiaJ Spranger, H Menger, S Mundlos, et al.Klinische Padiatrie|November 1, 1975
[Congenital spondylo-epiphyseal dysplasia: follow-up of a case over 9 years (author's transl)]T Luthardt, H Reinwein, H Schönenberg, et al.Archives of Gynecology and Obstetrics|August 29, 2002
Malformations in newborn: results based on 30,940 infants and fetuses from the Mainz congenital birth defect monitoring system (1990-1998)A Queisser-Luft, G Stolz, A Wiesel, et al.European Journal of Pediatrics|June 1, 1983
Heterogeneity of metatropic dysplasiaM Beck, M Roubicek, J G Rogers, et al.Journal of Inherited Metabolic Disease|January 1, 1981
Aspartylglycosaminuria in an Italian family: clinical and biochemical characteristicsJ Gehler, A C Sewell, C Becker, et al.Pageof 46