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M Siniscalco

Showing results (61-70 of 81) with videos related to

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American Journal of Human Genetics|April 1, 1990
Mental retardation in heterozygotes for the fragile-X mutation: evidence in favor of an X inactivation-dependent effectM Rocchi, N Archidiacono, A Rinaldi, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 1, 1989
Chromosomes of older humans are more prone to aminopterine-induced breakageD Esposito, G Fassina, P Szabo, et al.
American Journal of Medical Genetics|July 12, 1996
+2.71 LOD score at zero recombination is not sufficient for establishing linkage between X-linked mental retardation and X-chromosome markersR Robledo, P Melis, M Siniscalco, et al.
American Journal of Medical Genetics|November 6, 1995
X-linked ichthyosis without STS deficiency: clinical, genetical, and molecular studiesR Robledo, P Melis, E Schillinger, et al.
American Journal of Human Genetics|November 1, 1971
X-linkage of human phosphoglycerate kinase confirmed in man-mouse and man-Chinese hamster somatic cell hybridsP Meera Khan, A Westerveld, K H Grzeschik, et al.
Trends in Genetics : TIG|February 24, 2001
A plea to search for deletion polymorphism through genome scans in populationsM Siniscalco, R Robledo, S Orru, et al.
The EMBO Journal|March 1, 1985
The human genes for hemophilia A and hemophilia B flank the X chromosome fragile site at Xq27.3M Purrello, B Alhadeff, D Esposito, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 1, 1972
Cytological mapping of human X-linked genes by use of somatic cell hybrids involving an X-autosome translocation (mouse-hamster-human X-linked markers)K H Grzeschik, P W Allderdice, A Grzeschik, et al.
American Journal of Medical Genetics|September 15, 1991
Premutation for the Martin-Bell syndrome analyzed in a large pedigree segregating also for G6PD-deficiency. I: A working hypothesis on the nature of the FRAX-mutationsG Filippi, A Arslanian, F Dagna-Bricarelli, et al.
Science (New York, N.Y.)|December 20, 1985
A human Y-linked DNA polymorphism and its potential for estimating genetic and evolutionary distanceM Casanova, P Leroy, C Boucekkine, et al.
Pageof 9

Showing results (61-70 of 81) with videos related to

Sort By:
Pageof 9
American Journal of Human Genetics|April 1, 1990
Mental retardation in heterozygotes for the fragile-X mutation: evidence in favor of an X inactivation-dependent effectM Rocchi, N Archidiacono, A Rinaldi, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 1, 1989
Chromosomes of older humans are more prone to aminopterine-induced breakageD Esposito, G Fassina, P Szabo, et al.
American Journal of Medical Genetics|July 12, 1996
+2.71 LOD score at zero recombination is not sufficient for establishing linkage between X-linked mental retardation and X-chromosome markersR Robledo, P Melis, M Siniscalco, et al.
American Journal of Medical Genetics|November 6, 1995
X-linked ichthyosis without STS deficiency: clinical, genetical, and molecular studiesR Robledo, P Melis, E Schillinger, et al.
American Journal of Human Genetics|November 1, 1971
X-linkage of human phosphoglycerate kinase confirmed in man-mouse and man-Chinese hamster somatic cell hybridsP Meera Khan, A Westerveld, K H Grzeschik, et al.
Trends in Genetics : TIG|February 24, 2001
A plea to search for deletion polymorphism through genome scans in populationsM Siniscalco, R Robledo, S Orru, et al.
The EMBO Journal|March 1, 1985
The human genes for hemophilia A and hemophilia B flank the X chromosome fragile site at Xq27.3M Purrello, B Alhadeff, D Esposito, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 1, 1972
Cytological mapping of human X-linked genes by use of somatic cell hybrids involving an X-autosome translocation (mouse-hamster-human X-linked markers)K H Grzeschik, P W Allderdice, A Grzeschik, et al.
American Journal of Medical Genetics|September 15, 1991
Premutation for the Martin-Bell syndrome analyzed in a large pedigree segregating also for G6PD-deficiency. I: A working hypothesis on the nature of the FRAX-mutationsG Filippi, A Arslanian, F Dagna-Bricarelli, et al.
Science (New York, N.Y.)|December 20, 1985
A human Y-linked DNA polymorphism and its potential for estimating genetic and evolutionary distanceM Casanova, P Leroy, C Boucekkine, et al.
Pageof 9