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R Tenconi

Showing results (91-100 of 103) with videos related to

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Human Genetics|January 1, 1981
The "cat eye syndrome": dicentric small marker chromosome probably derived from a no.22 (tetrasomy 22pter to q11) associated with a characteristic phenotype. Report of 11 patients and delineation of the clinical pictureA Schinzel, W Schmid, M Fraccaro, et al.
Birth Defects Original Article Series|January 1, 1996
Congenital eye malformations: a descriptive epidemiologic study in about one million newborns in ItalyM Clementi, R Tenconi, F Bianchi, et al.
Lancet (London, England)|February 7, 2002
Chromosomal congenital anomalies and residence near hazardous waste landfill sitesM Vrijheid, H Dolk, B Armstrong, et al.
Cancer Research|November 11, 1998
STK11 mutations in Peutz-Jeghers syndrome and sporadic colon cancerN Resta, C Simone, C Mareni, et al.
American Journal of Medical Genetics|September 20, 2000
Genotype-phenotype correlations and clinical diagnostic criteria in Wolf-Hirschhorn syndromeM Zollino, C Di Stefano, G Zampino, et al.
American Journal of Medical Genetics|November 15, 2000
Cardiovascular malformations and other cardiovascular abnormalities in neurofibromatosis 1A E Lin, P H Birch, B R Korf, et al.
Human Mutation|April 24, 2001
Nine novel APC mutations in Italian FAP patientsN Resta, A Stella, F Susca, et al.
American Journal of Medical Genetics|June 9, 1999
Descriptive analysis of tibial pseudarthrosis in patients with neurofibromatosis 1D A Stevenson, P H Birch, J M Friedman, et al.
Human Genetics|August 14, 1998
The familial adenomatous polyposis region exhibits many different haplotypesA Stella, N Resta, A Polizzi, et al.
Journal of Medical Genetics|June 27, 2001
Cryptic telomeric rearrangements in subjects with mental retardation associated with dysmorphism and congenital malformationsE Rossi, F Piccini, M Zollino, et al.
Pageof 11

Showing results (91-100 of 103) with videos related to

Sort By:
Pageof 11
Human Genetics|January 1, 1981
The "cat eye syndrome": dicentric small marker chromosome probably derived from a no.22 (tetrasomy 22pter to q11) associated with a characteristic phenotype. Report of 11 patients and delineation of the clinical pictureA Schinzel, W Schmid, M Fraccaro, et al.
Birth Defects Original Article Series|January 1, 1996
Congenital eye malformations: a descriptive epidemiologic study in about one million newborns in ItalyM Clementi, R Tenconi, F Bianchi, et al.
Lancet (London, England)|February 7, 2002
Chromosomal congenital anomalies and residence near hazardous waste landfill sitesM Vrijheid, H Dolk, B Armstrong, et al.
Cancer Research|November 11, 1998
STK11 mutations in Peutz-Jeghers syndrome and sporadic colon cancerN Resta, C Simone, C Mareni, et al.
American Journal of Medical Genetics|September 20, 2000
Genotype-phenotype correlations and clinical diagnostic criteria in Wolf-Hirschhorn syndromeM Zollino, C Di Stefano, G Zampino, et al.
American Journal of Medical Genetics|November 15, 2000
Cardiovascular malformations and other cardiovascular abnormalities in neurofibromatosis 1A E Lin, P H Birch, B R Korf, et al.
Human Mutation|April 24, 2001
Nine novel APC mutations in Italian FAP patientsN Resta, A Stella, F Susca, et al.
American Journal of Medical Genetics|June 9, 1999
Descriptive analysis of tibial pseudarthrosis in patients with neurofibromatosis 1D A Stevenson, P H Birch, J M Friedman, et al.
Human Genetics|August 14, 1998
The familial adenomatous polyposis region exhibits many different haplotypesA Stella, N Resta, A Polizzi, et al.
Journal of Medical Genetics|June 27, 2001
Cryptic telomeric rearrangements in subjects with mental retardation associated with dysmorphism and congenital malformationsE Rossi, F Piccini, M Zollino, et al.
Pageof 11