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L Luzzatto

Showing results (151-160 of 259) with videos related to

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Human Genetics|January 1, 1980
Genetic heterogeneity of glucose 6-phosphate dehydrogenase deficiency in SardiniaU Testa, T Meloni, A Lania, et al.
Birth Defects Original Article Series|January 1, 1982
The pattern of thalassemia in NaplesG Pepe, L Lupi, A Mastrobuono, et al.
Clinical and Experimental Immunology|July 1, 1988
The establishment of cell lines from chronic B cell leukaemias: evidence of leukaemic origin by karyotypic abnormalities and Ig gene rearrangementJ V Melo, L Foroni, V Brito-Babapulle, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 1, 1990
Incomplete synthesis of N-glycans in congenital dyserythropoietic anemia type II caused by a defect in the gene encoding alpha-mannosidase IIM N Fukuda, K A Masri, A Dell, et al.
Gene Geography : a Computerized Bulletin on Human Gene Frequencies|April 1, 1996
DNA haplotypes in Africans and West Indians with sickle cell anaemia or SC diseaseK Konstantopoulos, T Vulliamy, D Swirsky, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|January 1, 1986
[Psychological aspects of thalassemia]P Massaglia, M T Pozzan, A Piga, et al.
Nucleic Acids Research|December 11, 1990
G6PD Canton a common deficient variant in South East Asia caused by a 459 Arg----Leu mutationD J Stevens, W Wanachiwanawin, P J Mason, et al.
The EMBO Journal|November 1, 1995
Targeted disruption of the housekeeping gene encoding glucose 6-phosphate dehydrogenase (G6PD): G6PD is dispensable for pentose synthesis but essential for defense against oxidative stressP P Pandolfi, F Sonati, R Rivi, et al.
Blood|February 1, 1989
Rearrangement of the T-cell receptor delta genes in human T-cell leukemiasL Foroni, M Laffan, T Boehm, et al.
Nature|March 14, 1991
Deficiency in red blood cellsD MacDonald, M Town, P Mason, et al.
Pageof 26

Showing results (151-160 of 259) with videos related to

Sort By:
Pageof 26
Human Genetics|January 1, 1980
Genetic heterogeneity of glucose 6-phosphate dehydrogenase deficiency in SardiniaU Testa, T Meloni, A Lania, et al.
Birth Defects Original Article Series|January 1, 1982
The pattern of thalassemia in NaplesG Pepe, L Lupi, A Mastrobuono, et al.
Clinical and Experimental Immunology|July 1, 1988
The establishment of cell lines from chronic B cell leukaemias: evidence of leukaemic origin by karyotypic abnormalities and Ig gene rearrangementJ V Melo, L Foroni, V Brito-Babapulle, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 1, 1990
Incomplete synthesis of N-glycans in congenital dyserythropoietic anemia type II caused by a defect in the gene encoding alpha-mannosidase IIM N Fukuda, K A Masri, A Dell, et al.
Gene Geography : a Computerized Bulletin on Human Gene Frequencies|April 1, 1996
DNA haplotypes in Africans and West Indians with sickle cell anaemia or SC diseaseK Konstantopoulos, T Vulliamy, D Swirsky, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|January 1, 1986
[Psychological aspects of thalassemia]P Massaglia, M T Pozzan, A Piga, et al.
Nucleic Acids Research|December 11, 1990
G6PD Canton a common deficient variant in South East Asia caused by a 459 Arg----Leu mutationD J Stevens, W Wanachiwanawin, P J Mason, et al.
The EMBO Journal|November 1, 1995
Targeted disruption of the housekeeping gene encoding glucose 6-phosphate dehydrogenase (G6PD): G6PD is dispensable for pentose synthesis but essential for defense against oxidative stressP P Pandolfi, F Sonati, R Rivi, et al.
Blood|February 1, 1989
Rearrangement of the T-cell receptor delta genes in human T-cell leukemiasL Foroni, M Laffan, T Boehm, et al.
Nature|March 14, 1991
Deficiency in red blood cellsD MacDonald, M Town, P Mason, et al.
Pageof 26