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Forabosco

Showing results (181-190 of 243) with videos related to

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Human Molecular Genetics|August 31, 2007
Loss of Wnt4 and Foxl2 leads to female-to-male sex reversal extending to germ cellsChris Ottolenghi, Emanuele Pelosi, Joseph Tran, et al.
Genomics|September 21, 2000
PLAC1, an Xq26 gene with placenta-specific expressionM Cocchia, R Huber, S Pantano, et al.
Prenatal Diagnosis|October 19, 2005
Detection of a novel dystrophin gene mutation through carrier analysis performed during prenatal diagnosis in a case with intragenic recombinationAntonio Percesepe, Maurizio Ferrari, Domenico Coviello, 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.
Human Genetics|October 30, 1999
CD4 and CD8 T lymphocyte inheritance. Evidence for major autosomal recessive genesM Clementi, P Forabosco, A Amadori, et al.
European Journal of Human Genetics : EJHG|November 28, 2000
Combined segregation and linkage analysis of inflammatory bowel disease in the IBD1 region using severity to characterise Crohn's disease and ulcerative colitis. On behalf of the GISCP Forabosco, A Collins, A Latiano, et al.
Chemical Senses|October 7, 2004
Bitter taste study in a sardinian genetic isolate supports the association of phenylthiocarbamide sensitivity to the TAS2R38 bitter receptor geneD A Prodi, D Drayna, P Forabosco, et al.
Archives of Dermatological Research|January 29, 2000
Autosomal dominant aplasia cutis congenita: report of a large Italian family and no hint for candidate chromosomal regionsM Fimiani, M Seri, P Rubegni, et al.
European Journal of Human Genetics : EJHG|November 28, 2000
Localisation of the gene responsible for fechtner syndrome in a region <600 Kb on 22q11-q13R Cusano, S Gangarossa, P Forabosco, 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.
Pageof 25

Showing results (181-190 of 243) with videos related to

Sort By:
Pageof 25
Human Molecular Genetics|August 31, 2007
Loss of Wnt4 and Foxl2 leads to female-to-male sex reversal extending to germ cellsChris Ottolenghi, Emanuele Pelosi, Joseph Tran, et al.
Genomics|September 21, 2000
PLAC1, an Xq26 gene with placenta-specific expressionM Cocchia, R Huber, S Pantano, et al.
Prenatal Diagnosis|October 19, 2005
Detection of a novel dystrophin gene mutation through carrier analysis performed during prenatal diagnosis in a case with intragenic recombinationAntonio Percesepe, Maurizio Ferrari, Domenico Coviello, 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.
Human Genetics|October 30, 1999
CD4 and CD8 T lymphocyte inheritance. Evidence for major autosomal recessive genesM Clementi, P Forabosco, A Amadori, et al.
European Journal of Human Genetics : EJHG|November 28, 2000
Combined segregation and linkage analysis of inflammatory bowel disease in the IBD1 region using severity to characterise Crohn's disease and ulcerative colitis. On behalf of the GISCP Forabosco, A Collins, A Latiano, et al.
Chemical Senses|October 7, 2004
Bitter taste study in a sardinian genetic isolate supports the association of phenylthiocarbamide sensitivity to the TAS2R38 bitter receptor geneD A Prodi, D Drayna, P Forabosco, et al.
Archives of Dermatological Research|January 29, 2000
Autosomal dominant aplasia cutis congenita: report of a large Italian family and no hint for candidate chromosomal regionsM Fimiani, M Seri, P Rubegni, et al.
European Journal of Human Genetics : EJHG|November 28, 2000
Localisation of the gene responsible for fechtner syndrome in a region <600 Kb on 22q11-q13R Cusano, S Gangarossa, P Forabosco, 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.
Pageof 25