Wanda Kuhl

发表

Some Mexican glucose-6-phosphate dehydrogenase variants revisited

E. Beutler, R. Lisker, Wanda Kuhl, 1991, Human Genetics.

Polymorphisms in African-Americans

E. Beutler, Wanda Kuhl, A. Kay, 2006 .

Linkage between a PvuII restriction fragment length polymorphism and G6PD A-202A/376G: evidence for a single origin of the common G6PD A — mutation

E. Beutler, Wanda Kuhl, 1990, Human Genetics.

Failure of Alglucerase Infused into Gaucher Disease Patients to Localize in Marrow Macrophages

E. Beutler, W. Kuhl, Wanda Kuhl, 1995, Molecular medicine.

Mutations in Jewish patients with Gaucher disease

E. Beutler, C. West, T. Gelbart, 1992 .

Studying X inactivation

E. Beutler, J. Curnutte, Wanda Kuhl, 1992, The Lancet.

The Molecular Biology of Gaucher Disease

E. Beutler, C. West, J. Sorge, 1988 .

Masking of Macrocytosis by α-Thalassemia in Blacks with Pernicious Anemia

E. Beutler, R. Carmel, Cage S. Johnson, 1982 .

Mutations in Jewish patients with Gaucher disease.

E. Beutler, A. Zimran, W. Kuhl, 1992, Blood.

Mutation analysis of glucose-6-phosphate dehydrogenase (G6PD) variants in Costa Rica

E. Beutler, Wanda Kuhl, G. F. Sáenz, 1991, Human Genetics.

DNA sequence abnormalities of human glucose-6-phosphate dehydrogenase variants.

L. Forman, E. Beutler, W. Kuhl, 1991, The Journal of biological chemistry.

Identification of the binding domain for NADP+ of human glucose-6-phosphate dehydrogenase by sequence analysis of mutants.

L. Forman, E. Beutler, W. Kuhl, 1989, Proceedings of the National Academy of Sciences of the United States of America.

Interference of heparin with the polymerase chain reaction.

E. Beutler, W. Kuhl, T. Gelbart, 1990, BioTechniques.

Human red cell glucose-6-phosphate dehydrogenase: All active enzyme has sequence predicted by the X chromosome-encoded cDNA

E. Beutler, T. Gelbart, Wanda Kuhl, 1990, Cell.

The NT 1311 polymorphism of G6PD: G6PD Mediterranean mutation may have originated independently in Europe and Asia.

E. Beutler, W. Kuhl, Wanda Kuhl, 1990, American journal of human genetics.

Homology between a human protein and a protein of the green garden pea.

E. Beutler, Pauline L. Lee, W. Kuhl, 1994, Genomics.

Identification of the second common Jewish Gaucher disease mutation makes possible population-based screening for the heterozygous state.

E. Beutler, W. Kuhl, C. West, 1991, Proceedings of the National Academy of Sciences of the United States of America.

The human glucocerebrosidase gene has two functional ATG initiator codons.

E. Beutler, W. Kuhl, C. West, 1987, American journal of human genetics.