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S Avigad

Showing results (41-50 of 67) with videos related to

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Harefuah|March 15, 1989
[Carrier detection and prenatal diagnosis in phenylketonuria, cystic fibrosis and adrenal hyperplasia use of molecular biology techniques]S Orgad, L Yaar, G Barkai, et al.
British Journal of Cancer|January 22, 2004
Molecular variants of the ATM gene in Hodgkin's disease in childrenE Liberzon, S Avigad, I Yaniv, et al.
Journal of Pediatric Gastroenterology and Nutrition|October 1, 1985
Assessment of intestinal and cardiorespiratory function in children with congenital heart disease on high-caloric formulasJ Yahav, S Avigad, M Frand, et al.
Israel Journal of Medical Sciences|August 1, 1994
Genetic alterations involving chromosome 1p in children with neuroblastomaS Avigad, Y Tamir, I Yaniv, et al.
Leukemia Research|August 1, 1997
Exon 5 mutations in the p53 gene in relapsed childhood acute lymphoblastic leukemiaO Blau, S Avigad, B Stark, et al.
American Journal of Human Genetics|August 1, 1991
Compound heterozygosity in nonphenylketonuria hyperphenylalanemia: the contribution of mutations for classical phenylketonuriaS Avigad, S Kleiman, M Weinstein, et al.
European Journal of Cancer (Oxford, England : 1990)|March 28, 1998
Prognostic relevance of genetic alterations in the p32 region of chromosome 1 in neuroblastomaS Avigad, H Benyaminy, Y Tamir, et al.
Lancet (London, England)|December 24, 1997
Synovial sarcoma of bone delineated by spectral karyotypingI J Cohen, J Issakov, S Avigad, et al.
Gut|January 1, 1980
Microvillous surface area in secondary disaccharidase deficiencyA D Phillips, S Avigad, J Sacks, et al.
Nature|March 8, 1990
A single origin of phenylketonuria in Yemenite JewsS Avigad, B E Cohen, S Bauer, et al.
Pageof 7

Showing results (41-50 of 67) with videos related to

Sort By:
Pageof 7
Harefuah|March 15, 1989
[Carrier detection and prenatal diagnosis in phenylketonuria, cystic fibrosis and adrenal hyperplasia use of molecular biology techniques]S Orgad, L Yaar, G Barkai, et al.
British Journal of Cancer|January 22, 2004
Molecular variants of the ATM gene in Hodgkin's disease in childrenE Liberzon, S Avigad, I Yaniv, et al.
Journal of Pediatric Gastroenterology and Nutrition|October 1, 1985
Assessment of intestinal and cardiorespiratory function in children with congenital heart disease on high-caloric formulasJ Yahav, S Avigad, M Frand, et al.
Israel Journal of Medical Sciences|August 1, 1994
Genetic alterations involving chromosome 1p in children with neuroblastomaS Avigad, Y Tamir, I Yaniv, et al.
Leukemia Research|August 1, 1997
Exon 5 mutations in the p53 gene in relapsed childhood acute lymphoblastic leukemiaO Blau, S Avigad, B Stark, et al.
American Journal of Human Genetics|August 1, 1991
Compound heterozygosity in nonphenylketonuria hyperphenylalanemia: the contribution of mutations for classical phenylketonuriaS Avigad, S Kleiman, M Weinstein, et al.
European Journal of Cancer (Oxford, England : 1990)|March 28, 1998
Prognostic relevance of genetic alterations in the p32 region of chromosome 1 in neuroblastomaS Avigad, H Benyaminy, Y Tamir, et al.
Lancet (London, England)|December 24, 1997
Synovial sarcoma of bone delineated by spectral karyotypingI J Cohen, J Issakov, S Avigad, et al.
Gut|January 1, 1980
Microvillous surface area in secondary disaccharidase deficiencyA D Phillips, S Avigad, J Sacks, et al.
Nature|March 8, 1990
A single origin of phenylketonuria in Yemenite JewsS Avigad, B E Cohen, S Bauer, et al.
Pageof 7