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Human Reproduction (Oxford, England)|December 20, 2005

Influence of intermediate and uninterrupted FMR1 CGG expansions in premature ovarian failure manifestationB Bodega, S Bione, L Dalprà, et al.

Cytogenetics and Cell Genetics|January 1, 1985

Localization of glucose-6-phosphate dehydrogenase in mouse and man by in situ hybridization: evidence for a single locus and transposition of homologous X-linked genesP A Martin-DeLeon, S F Wolf, G Persico, et al.

Proceedings of the National Academy of Sciences of the United States of America|December 1, 1993

Transcriptional organization of a 450-kb region of the human X chromosome in Xq28S Bione, F Tamanini, E Maestrini, et al.

Human Molecular Genetics|July 1, 1994

Isolation of new genes in distal Xq28: transcriptional map and identification of a human homologue of the ARD1 N-acetyl transferase of Saccharomyces cerevisiaeC Tribioli, M Mancini, E Plassart, et al.

Science (New York, N.Y.)|June 15, 1990

Fibroblast growth factor receptor is a portal of cellular entry for herpes simplex virus type 1R J Kaner, A Baird, A Mansukhani, et al.

Nucleic Acids Research|December 21, 1984

Complete concordance between glucose-6-phosphate dehydrogenase activity and hypomethylation of 3' CpG clusters: implications for X chromosome dosage compensationS F Wolf, S Dintzis, D Toniolo, et al.

American Journal of Medical Genetics|October 26, 2000

Mapping to distal Xq28 of nonspecific X-linked mental retardation MRX72: linkage analysis and clinical findings in a three-generation Sardinian familyS Russo, F Cogliati, F Cavalleri, et al.

Human Genetics|February 1, 1994

G6PD Ferrara I has the same two mutations as G6PD A(-) but a distinct biochemical phenotypeM D Cappellini, M Sampietro, D Toniolo, et al.

Proceedings of the National Academy of Sciences of the United States of America|November 25, 1998

Uncoupling signal transducers from oncogenic MET mutants abrogates cell transformation and inhibits invasive growthA Bardelli, P Longati, D Gramaglia, et al.

Clinical Genetics|October 23, 1997

X-linked severe mental retardation and a progressive neurological disorder in a Belgian family: clinical and genetic studiesS Claes, K Devriendt, P D'Adamo, et al.

Pageof 22

Showing results (151-160 of 214) with videos related to

Sort By:

Pageof 22

Human Reproduction (Oxford, England)|December 20, 2005

Influence of intermediate and uninterrupted FMR1 CGG expansions in premature ovarian failure manifestationB Bodega, S Bione, L Dalprà, et al.

Cytogenetics and Cell Genetics|January 1, 1985

Localization of glucose-6-phosphate dehydrogenase in mouse and man by in situ hybridization: evidence for a single locus and transposition of homologous X-linked genesP A Martin-DeLeon, S F Wolf, G Persico, et al.

Proceedings of the National Academy of Sciences of the United States of America|December 1, 1993

Transcriptional organization of a 450-kb region of the human X chromosome in Xq28S Bione, F Tamanini, E Maestrini, et al.

Human Molecular Genetics|July 1, 1994

Isolation of new genes in distal Xq28: transcriptional map and identification of a human homologue of the ARD1 N-acetyl transferase of Saccharomyces cerevisiaeC Tribioli, M Mancini, E Plassart, et al.

Science (New York, N.Y.)|June 15, 1990

Fibroblast growth factor receptor is a portal of cellular entry for herpes simplex virus type 1R J Kaner, A Baird, A Mansukhani, et al.

Nucleic Acids Research|December 21, 1984

Complete concordance between glucose-6-phosphate dehydrogenase activity and hypomethylation of 3' CpG clusters: implications for X chromosome dosage compensationS F Wolf, S Dintzis, D Toniolo, et al.

American Journal of Medical Genetics|October 26, 2000

Mapping to distal Xq28 of nonspecific X-linked mental retardation MRX72: linkage analysis and clinical findings in a three-generation Sardinian familyS Russo, F Cogliati, F Cavalleri, et al.

Human Genetics|February 1, 1994

G6PD Ferrara I has the same two mutations as G6PD A(-) but a distinct biochemical phenotypeM D Cappellini, M Sampietro, D Toniolo, et al.

Proceedings of the National Academy of Sciences of the United States of America|November 25, 1998

Uncoupling signal transducers from oncogenic MET mutants abrogates cell transformation and inhibits invasive growthA Bardelli, P Longati, D Gramaglia, et al.

Clinical Genetics|October 23, 1997

X-linked severe mental retardation and a progressive neurological disorder in a Belgian family: clinical and genetic studiesS Claes, K Devriendt, P D'Adamo, et al.

Pageof 22