Sfoglia per Autore
Close linkage of fragile X-mental retardation syndrome to haemophilia B and transmission through a normal male.
1983-01-01 Camerino, Giovanna; Mattei, Mg; Mattei, Jf; Jaye, M; Mandel, J. L.
Regional localization on the human X chromosome and polymorphism of the coagulation factor IX gene (hemophilia B locus).
1984-01-01 Camerino, Giovanna; Grzeschik, Kh; Jaye, M; DE LA SALLE, H; Tolstoshev, P; Lecocq, Jp; Heilig, R; Mandel, J. L.
Genetic mapping of the human X chromosome by using restriction fragment length polymorphisms.
1984-01-01 Drayna, D; Davies, K; Hartley, D; Mandel, Jl; Camerino, Giovanna; Williamson, R; White, R.
The telomeric region of the human X chromosome long arm: presence of a highly polymorphic DNA marker and analysis of recombination frequency.
1985-01-01 Oberle, I; Drayna, D; Camerino, Giovanna; White, R; Mandel, J. L.
Genetic screening for hemophilia A (classic hemophilia) with a polymorphic DNA probe.
1985-01-01 Oberle, I; Camerino, Giovanna; Heilig, R; Grunebaum, L; Cazenave, Jp; Crapanzano, C; Mannucci, Pm; Mandel, J. L.
Studies of the fragile site Xq28 by cytogenetic analysis and polymorphic DNA markers
1986-01-01 Raimondi, ELENA MARIA; Camerino, Giovanna; Romagnoni, M; Negri, R; Guglielmi, D; Berbenni, C; Lenti, C; Gambini, E; Musetti, L; De Carli, L.
Multipoint genetic mapping of the Xq26-q28 region in families with fragile X mental retardation and in normal families reveals tight linkage of markers in q26-q27.
1987-01-01 Oberlé, I; Camerino, Giovanna; Wrogemann, K; Arveiler, B; Hanauer, A; Raimondi, ELENA MARIA; Mandel, J. L.
A TaqI RFLP detecting single copy fragment (G80) from chromosome 7 p13-p15 (D7S373).
1987-01-01 Raimondi, ELENA MARIA; Bardoni, B; Rinaldi, E; Camerino, Giovanna
Genetic mapping of the Xq26-q28 region: tight linkage of loci in q26-27 and characterization of new markers useful for diagnostic applications
1987-01-01 Oberlè, I.; Arveiler, B.; Woelfin, A.; Camerino, Giovanna; Raimondi, ELENA MARIA; Hofker, M.; Pearson, P.; Mandel, J. L.
Isolation and characterization of a family of sequences dispersed on the human X chromosome.
1988-01-01 Bardoni, B; Guioli, S; Raimondi, ELENA MARIA; Heilig, R; Mandel, Jl; Ottolenghi, S; Camerino, Giovanna
Contiguous gene syndromes due to deletions in the distal short arm of the human X chromosome.
1989-01-01 Ballabio, A; Andria, G; Carrozzo, R; Persico, G; Bick, D; Campbell, L; Ropers, Hh; FERGUSON SMITH, Ma; Gimelli, G; Fraccaro, M; Maraschio, Paola; Zuffardi, Orsetta; Bardoni, B; Guioli, S; Camerino, Giovanna
A fragile understanding
1991-01-01 Camerino, Giovanna; Goodfellow, P.
A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal pathfinding molecules
1991-01-01 Franco, B; Guioli, S; Pragliola, A; Incerti, B; Bardoni, B; Tonlorenzi, R; Carrozzo, R; Maestrini, E; Pieretti, M; Taillonmiller, P; Brown, C; Willard, Hf; Lawrence, C; Persico, G; Camerino, Giovanna; Ballabio, A.
Kallmann syndrome gene on the X and Y chromosomes: implications for evolutionary divergence of human sex chromosomes.
1992-01-01 Incerti, B; Guioli, S; Pragliola, A; Zanaria, E; Borsani, G; Tonlorenzi, R; Bardoni, B; Franco, B; Wheeler, D; Ballabio, A; Camerino, Giovanna
Kallmann syndrome due to a translocation resulting in an X/Y fusion gene.
1992-01-01 Guioli, S; Incerti, B; Zanaria, E; Bardoni, B; Franco, B; Taylor, K; Ballabio, A; Camerino, Giovanna
An unusual member of the nuclear hormone receptor superfamily responsible for X-linked adrenal hypoplasia congenita.
1994-01-01 Zanaria, E; Muscatelli, F; Bardoni, B; Strom, T; Guioli, S; Guo, W; Lalli, E; Moser, C; Walker, A; Mccabe, Erb; Meitinger, T; Monaco, A; SASSONE CORSI, P; Camerino, Giovanna
A dosage sensitive locus at chromosome Xp21 is involved in male to female sex reversal.
1994-01-01 Bardoni, B.; Zanaria, E.; Guioli, S.; Floridia, G.; Worley, K. C.; Tonini, G.; Ferrante, E.; Chiumello, G.; Mccabe, E. R.; Fraccaro, M.; Zuffardi, Orsetta; Camerino, Giovanna
Mutations in the DAX-1 gene give rise to both X-linked adrenal hypoplasia congenita and hypogonadotropic hypogonadism
1994-01-01 Muscatelli, F; Strom, T; Walker, A. P.; Zanaria, E; Recan, D; Meindl, A; Bardoni, B; Guioli, S; Zehetner, G; Rabl, W; Schwarz, Hp; Kaplan, Jc; Camerino, Giovanna; Meitinger, T; Monaco, A.
A family of rapidly evolving genes from the sex reversal critical region in Xp21.
1995-01-01 Dabovic, B; Zanaria, E; Bardoni, B; Lisa, A; Bordignon, C; Russo, V; Matessi, C; Traversari, C; Camerino, Giovanna
Steroidogenic factor 1 and Dax-1 colocalize in multiple cell lineages: potential links in endocrine development.
1996-01-01 Ikeda, Y; Swain, A; Weber, Tj; Hentges, Ke; Zanaria, E; Lalli, E; Tamai, Kt; SASSONE CORSI, P; LOVELL BADGE, R; Camerino, Giovanna; Parker, K. L.
Titolo | Data di pubblicazione | Autore(i) | File |
---|---|---|---|
Close linkage of fragile X-mental retardation syndrome to haemophilia B and transmission through a normal male. | 1-gen-1983 | Camerino, Giovanna; Mattei, Mg; Mattei, Jf; Jaye, M; Mandel, J. L. | |
Regional localization on the human X chromosome and polymorphism of the coagulation factor IX gene (hemophilia B locus). | 1-gen-1984 | Camerino, Giovanna; Grzeschik, Kh; Jaye, M; DE LA SALLE, H; Tolstoshev, P; Lecocq, Jp; Heilig, R; Mandel, J. L. | |
Genetic mapping of the human X chromosome by using restriction fragment length polymorphisms. | 1-gen-1984 | Drayna, D; Davies, K; Hartley, D; Mandel, Jl; Camerino, Giovanna; Williamson, R; White, R. | |
The telomeric region of the human X chromosome long arm: presence of a highly polymorphic DNA marker and analysis of recombination frequency. | 1-gen-1985 | Oberle, I; Drayna, D; Camerino, Giovanna; White, R; Mandel, J. L. | |
Genetic screening for hemophilia A (classic hemophilia) with a polymorphic DNA probe. | 1-gen-1985 | Oberle, I; Camerino, Giovanna; Heilig, R; Grunebaum, L; Cazenave, Jp; Crapanzano, C; Mannucci, Pm; Mandel, J. L. | |
Studies of the fragile site Xq28 by cytogenetic analysis and polymorphic DNA markers | 1-gen-1986 | Raimondi, ELENA MARIA; Camerino, Giovanna; Romagnoni, M; Negri, R; Guglielmi, D; Berbenni, C; Lenti, C; Gambini, E; Musetti, L; De Carli, L. | |
Multipoint genetic mapping of the Xq26-q28 region in families with fragile X mental retardation and in normal families reveals tight linkage of markers in q26-q27. | 1-gen-1987 | Oberlé, I; Camerino, Giovanna; Wrogemann, K; Arveiler, B; Hanauer, A; Raimondi, ELENA MARIA; Mandel, J. L. | |
A TaqI RFLP detecting single copy fragment (G80) from chromosome 7 p13-p15 (D7S373). | 1-gen-1987 | Raimondi, ELENA MARIA; Bardoni, B; Rinaldi, E; Camerino, Giovanna | |
Genetic mapping of the Xq26-q28 region: tight linkage of loci in q26-27 and characterization of new markers useful for diagnostic applications | 1-gen-1987 | Oberlè, I.; Arveiler, B.; Woelfin, A.; Camerino, Giovanna; Raimondi, ELENA MARIA; Hofker, M.; Pearson, P.; Mandel, J. L. | |
Isolation and characterization of a family of sequences dispersed on the human X chromosome. | 1-gen-1988 | Bardoni, B; Guioli, S; Raimondi, ELENA MARIA; Heilig, R; Mandel, Jl; Ottolenghi, S; Camerino, Giovanna | |
Contiguous gene syndromes due to deletions in the distal short arm of the human X chromosome. | 1-gen-1989 | Ballabio, A; Andria, G; Carrozzo, R; Persico, G; Bick, D; Campbell, L; Ropers, Hh; FERGUSON SMITH, Ma; Gimelli, G; Fraccaro, M; Maraschio, Paola; Zuffardi, Orsetta; Bardoni, B; Guioli, S; Camerino, Giovanna | |
A fragile understanding | 1-gen-1991 | Camerino, Giovanna; Goodfellow, P. | |
A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal pathfinding molecules | 1-gen-1991 | Franco, B; Guioli, S; Pragliola, A; Incerti, B; Bardoni, B; Tonlorenzi, R; Carrozzo, R; Maestrini, E; Pieretti, M; Taillonmiller, P; Brown, C; Willard, Hf; Lawrence, C; Persico, G; Camerino, Giovanna; Ballabio, A. | |
Kallmann syndrome gene on the X and Y chromosomes: implications for evolutionary divergence of human sex chromosomes. | 1-gen-1992 | Incerti, B; Guioli, S; Pragliola, A; Zanaria, E; Borsani, G; Tonlorenzi, R; Bardoni, B; Franco, B; Wheeler, D; Ballabio, A; Camerino, Giovanna | |
Kallmann syndrome due to a translocation resulting in an X/Y fusion gene. | 1-gen-1992 | Guioli, S; Incerti, B; Zanaria, E; Bardoni, B; Franco, B; Taylor, K; Ballabio, A; Camerino, Giovanna | |
An unusual member of the nuclear hormone receptor superfamily responsible for X-linked adrenal hypoplasia congenita. | 1-gen-1994 | Zanaria, E; Muscatelli, F; Bardoni, B; Strom, T; Guioli, S; Guo, W; Lalli, E; Moser, C; Walker, A; Mccabe, Erb; Meitinger, T; Monaco, A; SASSONE CORSI, P; Camerino, Giovanna | |
A dosage sensitive locus at chromosome Xp21 is involved in male to female sex reversal. | 1-gen-1994 | Bardoni, B.; Zanaria, E.; Guioli, S.; Floridia, G.; Worley, K. C.; Tonini, G.; Ferrante, E.; Chiumello, G.; Mccabe, E. R.; Fraccaro, M.; Zuffardi, Orsetta; Camerino, Giovanna | |
Mutations in the DAX-1 gene give rise to both X-linked adrenal hypoplasia congenita and hypogonadotropic hypogonadism | 1-gen-1994 | Muscatelli, F; Strom, T; Walker, A. P.; Zanaria, E; Recan, D; Meindl, A; Bardoni, B; Guioli, S; Zehetner, G; Rabl, W; Schwarz, Hp; Kaplan, Jc; Camerino, Giovanna; Meitinger, T; Monaco, A. | |
A family of rapidly evolving genes from the sex reversal critical region in Xp21. | 1-gen-1995 | Dabovic, B; Zanaria, E; Bardoni, B; Lisa, A; Bordignon, C; Russo, V; Matessi, C; Traversari, C; Camerino, Giovanna | |
Steroidogenic factor 1 and Dax-1 colocalize in multiple cell lineages: potential links in endocrine development. | 1-gen-1996 | Ikeda, Y; Swain, A; Weber, Tj; Hentges, Ke; Zanaria, E; Lalli, E; Tamai, Kt; SASSONE CORSI, P; LOVELL BADGE, R; Camerino, Giovanna; Parker, K. L. |
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