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R Tenconi

Showing results (81-90 of 103) with videos related to

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Human Genetics|October 30, 1999
CD4 and CD8 T lymphocyte inheritance. Evidence for major autosomal recessive genesM Clementi, P Forabosco, A Amadori, et al.
Annales De Genetique|June 1, 1976
[Localization of the gene of the glyceraldehyde 3 phosphate dehydrogenase on the distal segment of the short arm of the chromosome 12]M O Rethoré, C Junien, G Malpuech, et al.
Teratology|January 1, 1993
Omphalocele and gastroschisis: a collaborative study of five Italian congenital malformation registriesE Calzolari, S Volpato, F Bianchi, et al.
Human Genetics|October 1, 1993
D8S7 is consistently deleted in inverted duplications of the short arm of chromosome 8 (inv dup 8p)A Minelli, G Floridia, E Rossi, et al.
Journal of Medical Genetics|January 20, 2004
Mental retardation and cardiovascular malformations in NF1 microdeleted patients point to candidate genes in 17q11.2M Venturin, P Guarnieri, F Natacci, et al.
Journal of Medical Screening|February 24, 2001
Evaluation of the prenatal diagnosis of neural tube defects by fetal ultrasonographic examination in different centres across EuropeP A Boyd, D G Wellesley, H E De Walle, et al.
Human Genetics|January 1, 1985
Frequency of consanguineous marriages among parents and grandparents of Down patientsM Devoto, L Prosperi, F D Bricarelli, et al.
Human Genetics|January 7, 1998
Clinical and genetic heterogeneity in Meckel syndromeP Paavola, R Salonen, A Baumer, et al.
American Journal of Human Genetics|January 13, 2000
NF1 microdeletion syndrome: refined FISH characterization of sporadic and familial deletions with locus-specific probesP Riva, L Corrado, F Natacci, et al.
Lancet (London, England)|August 26, 1998
Risk of congenital anomalies near hazardous-waste landfill sites in Europe: the EUROHAZCON studyH Dolk, M Vrijheid, B Armstrong, et al.
Pageof 11

Showing results (81-90 of 103) with videos related to

Sort By:
Pageof 11
Human Genetics|October 30, 1999
CD4 and CD8 T lymphocyte inheritance. Evidence for major autosomal recessive genesM Clementi, P Forabosco, A Amadori, et al.
Annales De Genetique|June 1, 1976
[Localization of the gene of the glyceraldehyde 3 phosphate dehydrogenase on the distal segment of the short arm of the chromosome 12]M O Rethoré, C Junien, G Malpuech, et al.
Teratology|January 1, 1993
Omphalocele and gastroschisis: a collaborative study of five Italian congenital malformation registriesE Calzolari, S Volpato, F Bianchi, et al.
Human Genetics|October 1, 1993
D8S7 is consistently deleted in inverted duplications of the short arm of chromosome 8 (inv dup 8p)A Minelli, G Floridia, E Rossi, et al.
Journal of Medical Genetics|January 20, 2004
Mental retardation and cardiovascular malformations in NF1 microdeleted patients point to candidate genes in 17q11.2M Venturin, P Guarnieri, F Natacci, et al.
Journal of Medical Screening|February 24, 2001
Evaluation of the prenatal diagnosis of neural tube defects by fetal ultrasonographic examination in different centres across EuropeP A Boyd, D G Wellesley, H E De Walle, et al.
Human Genetics|January 1, 1985
Frequency of consanguineous marriages among parents and grandparents of Down patientsM Devoto, L Prosperi, F D Bricarelli, et al.
Human Genetics|January 7, 1998
Clinical and genetic heterogeneity in Meckel syndromeP Paavola, R Salonen, A Baumer, et al.
American Journal of Human Genetics|January 13, 2000
NF1 microdeletion syndrome: refined FISH characterization of sporadic and familial deletions with locus-specific probesP Riva, L Corrado, F Natacci, et al.
Lancet (London, England)|August 26, 1998
Risk of congenital anomalies near hazardous-waste landfill sites in Europe: the EUROHAZCON studyH Dolk, M Vrijheid, B Armstrong, et al.
Pageof 11