Automata for the assessment of knowledge von Dowling, C.E., Hockemeyer, C.

Volltext

Characterization of β-thalassaemia mutations using direct genomic sequencing of amplified single copy DNA von Wong, Corinne, Dowling, Carol E, Saiki, Randall K, Higuchi, Russell G, Erlich, Henry A, Kazazian, Haig H

Volltext

Evolution of a Genetic Disease in an Ethnic Isolate: β-Thalassemia in the Jews of Kurdistan von Rund, Deborah, Cohen, Tirza, Filon, Dvora, Dowling, Carol E., Warren, Tina C., Barak, Igal, Rachmilewitz, Eliezer, Kazazian, Haig H., Oppenheim, Ariella

Volltext

On the Irredundant Generation of Knowledge Spaces von Dowling, Cornelia E.

Volltext

Dominant Thalassemia-like Phenotypes Associated With Mutations in Exon 3 of the β-Globin Gene von Kazazian, Haig H., Dowling, Carol E., Hurwitz, Richard L., Coleman, Morton, Stopeck, Alison, Adams III, Junius G.

Volltext

A PSEUDODEFICIENCY ALLELE COMMON IN NON-JEWISH TAY-SACHS CARRIERS - IMPLICATIONS FOR CARRIER SCREENING von TRIGGSRAINE, BL, MULES, EH, KABACK, MM, LIMSTEELE, JST, DOWLING, CE, AKERMAN, BR, NATOWICZ, MR, GREBNER, EE, NAVON, R, WELCH, JP, GREENBERG, CR, THOMAS, GH, GRAVEL, RA

Volltext

Applying the Basis of a Knowledge Space for Controlling the Questioning of an Expert von Dowling, Cornelia E.

Volltext

Validity of Spaces for Assessing Knowledge about Fractions von Baumunk, Katja, Dowling†, Cornelia E

Volltext

The Spectrum of β-Thalassemia Genes in China and Southeast Asia von Kazazian, Haig H., Dowling, Carol E., Waber, Pamela G., Huang, Shangzhi, Lo, Wilson H.Y.

Volltext

The spectrum of beta-thalassemia genes in China and Southeast Asia von Kazazian, HH Jr, Dowling, CE, Waber, PG, Huang, S, Lo, WH

Volltext

Hinf I polymorphism 3' to the human β-globin gene detected by the polymerase chain reaction (PCR) von SEMENZA, G. L, DOWLING, C. E, KAZAZIAN, H. H. JR

Volltext

Homozygous β-Thalassemia Without Anemia von Safaya, S., Rieder, R.F., Dowling, C.E., Kazazian Jr, H.H., Adams III, J.G.

Volltext

Gene Defects in β-Thalassemia and Their Prenatal Diagnosis von KAZAZIAN JR, HAIG H., DOWLING, CAROL E., BOEHM, CORINNE D., WARREN, TINA C., ECONOMOU, EFFROSINI P., KATZ, JOEL, ANTONARAKIS, STYLIANOS E.

Volltext

Hemoglobin Bart's Disease in an Italian Boy: Interaction between α-Thalassemia and Hereditary Persistence of Fetal Hemoglobin von Chui, David H.K, Patterson, Margaret, Dowling, Carol E, Kazazian, Haig H, Kendall, Alan G

Volltext

Characterization of a spontaneous mutation to a β-thalassemia allele von KAZAZIAN, H. H. JR, ORKIN, S. H, BOEHM, C. D, GOFF, S. C, WONG, C, DOWLING, C. E, NEWBURGER, P. E, KNOWLTON, R. G, BROWN, V, DONIS-KELLER, H

Volltext

A novel mutation in the invariant AG of the acceptor splice site of intron 4 of the beta -hexosaminidase alpha -subunit gene in two unrelated American black G sub(M2)-gangliosidosi... von Mules, E H, Dowling, CE, Petersen, M B, Kazazian, HH Jr, Thomas, G H

Volltext

Prenatal Diagnosis of Sickle Cell Anemia-1988 von KAZAZIAN JR, HAIG H., PHILLIPS, DEBORAH G., DOWLING, CAROL E., BOEHM, CORINNE D.

Volltext

Prenatal Diagnosis of Hemoglobinopathies by DNA Analysis von KAZAZIAN JR, HAIG H., BOEHM, CORINNE D., DOWLING, CAROL E.

Volltext

Evidence supporting a single origin of the beta super(C)-globin gene in blacks von Boehm, C D, Dowling, CE, Antonarakis, SE, Honig, G R, Kazazian, HH Jr

Volltext

Use of oligonucleotide hybridization in the characterization of a beta zero-thalassemia gene (beta 37 TGG----TGA) in a Saudi Arabian family von Boehm, C D, Dowling, C E, Waber, P G, Giardina, P J, Kazazian, Jr, H H

Volltext