L Luzzatto|S M Gartler - JoVE Visualize

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The Journal of Investigative Dermatology|May 1, 1991

Analysis of beta, gamma, and delta T-cell receptor genes in lymphomatoid papulosis: cellular basis of two distinct histologic subsetsS Whittaker, N Smith, R R Jones, et al.

Human Molecular Genetics|November 1, 1992

Methylation analysis of CGG sites in the CpG island of the human FMR1 geneR S Hansen, S M Gartler, C R Scott, et al.

Proceedings of the National Academy of Sciences of the United States of America|October 1, 1987

High rate of recombination and double crossovers in the mouse pseudoautosomal region during male meiosisP Soriano, E A Keitges, D F Schorderet, et al.

Proceedings of the National Academy of Sciences of the United States of America|November 1, 1990

Polymerase chain reaction-aided genomic sequencing of an X chromosome-linked CpG island: methylation patterns suggest clonal inheritance, CpG site autonomy, and an explanation of activity state stabilityG P Pfeifer, S D Steigerwald, R S Hansen, et al.

Cell|July 2, 1993

Association of fragile X syndrome with delayed replication of the FMR1 geneR S Hansen, T K Canfield, M M Lamb, et al.

Proceedings of the National Academy of Sciences of the United States of America|June 6, 1998

Reactivation of XIST in normal fibroblasts and a somatic cell hybrid: abnormal localization of XIST RNA in hybrid cellsR S Hansen, T K Canfield, A M Stanek, et al.

Human Molecular Genetics|June 1, 1992

Both mutations in G6PD A- are necessary to produce the G6PD deficient phenotypeM Town, J M Bautista, P J Mason, et al.

Acta Cytologica|March 1, 1996

Psammoma bodies and cells from in situ fallopian tube carcinoma in endometrial smears: a case reportR Luzzatto, G Sisson, L Luzzatto, et al.

Acta Haematologica|January 1, 1976

Erythrocyte enzymes in neonatal juandiceU Bienzle, C E Effiong, V E Aimaku, et al.

British Journal of Haematology|June 1, 1994

Myelodysplasia in a patient with pre-existing paroxysmal nocturnal haemoglobinuria: a clonal disease originating from within a clonal diseaseL Longo, M Bessler, P Beris, et al.

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Showing results (101-110 of 237) with videos related to

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The Journal of Investigative Dermatology|May 1, 1991

Analysis of beta, gamma, and delta T-cell receptor genes in lymphomatoid papulosis: cellular basis of two distinct histologic subsetsS Whittaker, N Smith, R R Jones, et al.

Human Molecular Genetics|November 1, 1992

Methylation analysis of CGG sites in the CpG island of the human FMR1 geneR S Hansen, S M Gartler, C R Scott, et al.

Proceedings of the National Academy of Sciences of the United States of America|October 1, 1987

High rate of recombination and double crossovers in the mouse pseudoautosomal region during male meiosisP Soriano, E A Keitges, D F Schorderet, et al.

Proceedings of the National Academy of Sciences of the United States of America|November 1, 1990

Polymerase chain reaction-aided genomic sequencing of an X chromosome-linked CpG island: methylation patterns suggest clonal inheritance, CpG site autonomy, and an explanation of activity state stabilityG P Pfeifer, S D Steigerwald, R S Hansen, et al.

Cell|July 2, 1993

Association of fragile X syndrome with delayed replication of the FMR1 geneR S Hansen, T K Canfield, M M Lamb, et al.

Proceedings of the National Academy of Sciences of the United States of America|June 6, 1998

Reactivation of XIST in normal fibroblasts and a somatic cell hybrid: abnormal localization of XIST RNA in hybrid cellsR S Hansen, T K Canfield, A M Stanek, et al.

Human Molecular Genetics|June 1, 1992

Both mutations in G6PD A- are necessary to produce the G6PD deficient phenotypeM Town, J M Bautista, P J Mason, et al.

Acta Cytologica|March 1, 1996

Psammoma bodies and cells from in situ fallopian tube carcinoma in endometrial smears: a case reportR Luzzatto, G Sisson, L Luzzatto, et al.

Acta Haematologica|January 1, 1976

Erythrocyte enzymes in neonatal juandiceU Bienzle, C E Effiong, V E Aimaku, et al.

British Journal of Haematology|June 1, 1994

Myelodysplasia in a patient with pre-existing paroxysmal nocturnal haemoglobinuria: a clonal disease originating from within a clonal diseaseL Longo, M Bessler, P Beris, et al.

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