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A Forabosco

Showing results (121-130 of 134) with videos related to

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Genomics|September 21, 2000
PLAC1, an Xq26 gene with placenta-specific expressionM Cocchia, R Huber, S Pantano, et al.
Human Mutation|January 1, 1994
A new mutation (TTR Ala-47) in the transthyretin gene associated with hereditary amyloidosisA Ferlini, M C Patrosso, M Repetto, et al.
Genomics|September 19, 2001
X/autosomal translocations in the Xq critical region associated with premature ovarian failure fall within and outside genesS Mumm, L Herrera, P W Waeltz, et al.
Ophthalmic Paediatrics and Genetics|March 1, 1993
Transthyretin-related TTR hereditary amyloidosis of the vitreous body. Clinical and molecular characterization in two Italian familiesF Salvi, G Salvi, R Volpe, et al.
Human Molecular Genetics|April 18, 1998
A novel pseudoautosomal gene encoding a putative GTP-binding protein resides in the vicinity of the Xp/Yp telomereF Gianfrancesco, T Esposito, L Montanini, et al.
Genome Research|December 4, 2001
Differential divergence of three human pseudoautosomal genes and their mouse homologs: implications for sex chromosome evolutionF Gianfrancesco, R Sanges, T Esposito, et al.
European Journal of Human Genetics : EJHG|March 14, 2000
Opposite deletions/duplications of the X chromosome: two novel reciprocal rearrangementsS Giglio, B Pirola, G Arrigo, et al.
Gene|March 18, 1997
Mapping of 59 EST gene markers in 31 intervals spanning the human X chromosomeF Gianfrancesco, T Esposito, L Ruini, et al.
Cytometry|April 23, 1999
Fetal erythroblast isolation up to purity from cord blood and their culture in vitroG Sitar, S Garagna, M Zuccotti, et al.
Nature Genetics|March 1, 1996
Mutations in GPC3, a glypican gene, cause the Simpson-Golabi-Behmel overgrowth syndromeG Pilia, R M Hughes-Benzie, A MacKenzie, et al.
Pageof 14

Showing results (121-130 of 134) with videos related to

Sort By:
Pageof 14
Genomics|September 21, 2000
PLAC1, an Xq26 gene with placenta-specific expressionM Cocchia, R Huber, S Pantano, et al.
Human Mutation|January 1, 1994
A new mutation (TTR Ala-47) in the transthyretin gene associated with hereditary amyloidosisA Ferlini, M C Patrosso, M Repetto, et al.
Genomics|September 19, 2001
X/autosomal translocations in the Xq critical region associated with premature ovarian failure fall within and outside genesS Mumm, L Herrera, P W Waeltz, et al.
Ophthalmic Paediatrics and Genetics|March 1, 1993
Transthyretin-related TTR hereditary amyloidosis of the vitreous body. Clinical and molecular characterization in two Italian familiesF Salvi, G Salvi, R Volpe, et al.
Human Molecular Genetics|April 18, 1998
A novel pseudoautosomal gene encoding a putative GTP-binding protein resides in the vicinity of the Xp/Yp telomereF Gianfrancesco, T Esposito, L Montanini, et al.
Genome Research|December 4, 2001
Differential divergence of three human pseudoautosomal genes and their mouse homologs: implications for sex chromosome evolutionF Gianfrancesco, R Sanges, T Esposito, et al.
European Journal of Human Genetics : EJHG|March 14, 2000
Opposite deletions/duplications of the X chromosome: two novel reciprocal rearrangementsS Giglio, B Pirola, G Arrigo, et al.
Gene|March 18, 1997
Mapping of 59 EST gene markers in 31 intervals spanning the human X chromosomeF Gianfrancesco, T Esposito, L Ruini, et al.
Cytometry|April 23, 1999
Fetal erythroblast isolation up to purity from cord blood and their culture in vitroG Sitar, S Garagna, M Zuccotti, et al.
Nature Genetics|March 1, 1996
Mutations in GPC3, a glypican gene, cause the Simpson-Golabi-Behmel overgrowth syndromeG Pilia, R M Hughes-Benzie, A MacKenzie, et al.
Pageof 14