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Journal of Medical Genetics|July 1, 1997
A case of apparent trisomy 21 without the Down's syndrome phenotypeD Avramopoulos, I Kennerknecht, G Barbi, et al.American Journal of Medical Genetics|July 1, 1991
Chromosome instability and X-ray hypersensitivity in a microcephalic and growth-retarded childG Barbi, J M Scheres, D Schindler, et al.Prenatal Diagnosis|December 17, 1998
Further observations of true mosaic trisomy 17 ascertained in amniotic fluid cell culturesM Djalali, G Barbi, J Mueller-Navia, et al.Human Genetics|November 1, 1993
Molecular analysis of mutations in the gene FMR-1 segregating in fragile X familiesP Steinbach, D Wöhrle, G Tariverdian, et al.Bone Marrow Transplantation|December 26, 2001
Eradication of a dysfunctional HLA-haploidentical T cell system by a second HLA-identical BMTM Ege, B J Manfras, G Barbi, et al.European Journal of Pediatrics|October 1, 1992
Simultaneous measurement, using flow cytometry, of radiosensitivity and defective mitogen response in ataxia telangiectasia and related syndromesH Seyschab, D Schindler, R Friedl, et al.American Journal of Medical Genetics|October 23, 1995
Agonadism in two sisters with XY gonosomal constitution, mental retardation, short stature, severely retarded bone age, and multiple extragenital malformations: a new autosomal recessive syndromeI Kennerknecht, P von Saurma, R Brenner, et al.American Journal of Human Genetics|August 1, 1992
A microdeletion of less than 250 kb, including the proximal part of the FMR-I gene and the fragile-X site, in a male with the clinical phenotype of fragile-X syndromeD Wöhrle, D Kotzot, M C Hirst, et al.International Journal of Cancer|March 13, 1999
Detailed marker chromosome analysis in cell line U-BLC1, established from transitional-cell carcinoma of the bladderJ Bruch, G Wöhr, S Brüderlein, et al.American Journal of Medical Genetics|April 1, 1992
Collaborative prospective study of the fragile X syndrome: one-year progress reportS L Sherman, G Barbi, K Brøndum-Nielsen, et al.Pageof 6