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Human Genetics|January 1, 1985
Folic acid sensitive fragile sites are not limited to the human karyotype. Demonstration of nonrandom gaps and breaks in the Persian vole Ellobius lutescens Th. inducible by methotrexate, fluorodeoxyuridine, and aphidicolinM Djalali, G Barbi, P SteinbachLa Clinica Terapeutica|March 31, 1989
[Pantethine, diabetes mellitus and atherosclerosis. Clinical study of 1045 patients]C Donati, R S Bertieri, G BarbiAmerican Journal of Medical Genetics|February 1, 1991
How can the frequency of false-negative findings in prenatal diagnoses of fra(X) be reduced: experience with first trimester chorionic villi samplingI Kennerknecht, G Barbi, N Dahl, et al.Journal of Medical Genetics|August 1, 1997
"Cutis tricolor": congenital hyper- and hypopigmented macules associated with a sporadic multisystem birth defect: an unusual example of twin spotting?R Happle, G Barbi, D Eckert, et al.Human Genetics|December 1, 1990
Heterozygous expression of X-linked chondrodysplasia punctata. Complex chromosome aberration including deletion of MIC2 and STSD Wöhrle, G Barbi, W Schulz, et al.Human Genetics|January 1, 1983
Expression of the fragile site Xq27 in fibroblasts. I. Detection of fra(X)(q27) in fibroblast clones from males with X-linked mental retardationP Steinbach, G Barbi, S Baur, et al.Human Genetics|January 1, 1983
Expression of the fragile site Xq27 in fibroblasts. II. Evidence for negative and positive clones from heterozygous females and possible relationship between frequency and phenotypeP Steinbach, G Barbi, S Baur, et al.Human Genetics|January 1, 1983
Manifestation of the fragile site Xq27 in fibroblasts. III. A method to demonstrate R-type replication patterns and the fragile siteG Barbi, P Steinbach, A Wiedenmann, et al.Prenatal Diagnosis|August 1, 1992
Introduction of early amniocentesis to routine prenatal diagnosisM Djalali, G Barbi, I Kennerknecht, et al.Human Genetics|January 1, 1985
Manifestation of the fragile site Xq27 in fibroblasts. IV. Clones from a heterozygous female do not manifest this site homogeneously on either the early or late replicating X chromosomeG Barbi, P Steinbach, S Baur, et al.Pageof 6