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Forabosco

Showing results (161-170 of 243) with videos related to

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Nature Communications|May 16, 2013
Constitutively active Foxo3 in oocytes preserves ovarian reserve in miceEmanuele Pelosi, Shakib Omari, Marc Michel, et al.
Annales De Genetique|March 1, 1975
Partial 4q trisomy. Apropos of 3 casesB Dutrillaux, C Laurent, A Forabosco, et al.
International Journal of Tissue Reactions|January 1, 1993
Human neonatal ovary: proposal of a three-dimensional modelV F Ferrario, L Marzona, C Sforza, et al.
Helvetica Paediatrica Acta|August 1, 1988
Heart disease in Turner's syndromeL Mazzanti, D Prandstraller, D Tassinari, et al.
Annals of Human Genetics|May 1, 1997
Segregation analysis of ovarian cancer using diathesis to include other cancersD M Eccles, P Forabosco, A Williams, et al.
American Journal of Medical Genetics. Part A|August 19, 2007
Pure segmental trisomy 1q42-qter in a boy with a severe phenotypeAntonio Percesepe, Licia Lugli, Mauro Pierluigi, et al.
Human Heredity|May 8, 2007
Data acquisition for meta-analysis of genome-wide linkage studies using the genome search meta-analysis methodPaola Forabosco, Mandy Y M Ng, Emmanuelle Bouzigon, et al.
Prenatal Diagnosis|August 12, 2004
First-trimester prenatal screening for the common 35delG GJB2 mutation causing prelingual deafnessDomenico A Coviello, Bruno Brambati, Lucia Tului, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|May 4, 2010
Unexpected phenotype in a boy with trisomy of the SHOX geneLorenzo Iughetti, Lucia Capone, Heba Elsedfy, et al.
Journal of Medical Genetics|May 16, 2002
Association of Crohn's disease and ulcerative colitis with haplotypes of the MLH1 gene in Italian inflammatory bowel disease patientsV Annese, A Piepoli, A Andriulli, et al.
Pageof 25

Showing results (161-170 of 243) with videos related to

Sort By:
Pageof 25
Nature Communications|May 16, 2013
Constitutively active Foxo3 in oocytes preserves ovarian reserve in miceEmanuele Pelosi, Shakib Omari, Marc Michel, et al.
Annales De Genetique|March 1, 1975
Partial 4q trisomy. Apropos of 3 casesB Dutrillaux, C Laurent, A Forabosco, et al.
International Journal of Tissue Reactions|January 1, 1993
Human neonatal ovary: proposal of a three-dimensional modelV F Ferrario, L Marzona, C Sforza, et al.
Helvetica Paediatrica Acta|August 1, 1988
Heart disease in Turner's syndromeL Mazzanti, D Prandstraller, D Tassinari, et al.
Annals of Human Genetics|May 1, 1997
Segregation analysis of ovarian cancer using diathesis to include other cancersD M Eccles, P Forabosco, A Williams, et al.
American Journal of Medical Genetics. Part A|August 19, 2007
Pure segmental trisomy 1q42-qter in a boy with a severe phenotypeAntonio Percesepe, Licia Lugli, Mauro Pierluigi, et al.
Human Heredity|May 8, 2007
Data acquisition for meta-analysis of genome-wide linkage studies using the genome search meta-analysis methodPaola Forabosco, Mandy Y M Ng, Emmanuelle Bouzigon, et al.
Prenatal Diagnosis|August 12, 2004
First-trimester prenatal screening for the common 35delG GJB2 mutation causing prelingual deafnessDomenico A Coviello, Bruno Brambati, Lucia Tului, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|May 4, 2010
Unexpected phenotype in a boy with trisomy of the SHOX geneLorenzo Iughetti, Lucia Capone, Heba Elsedfy, et al.
Journal of Medical Genetics|May 16, 2002
Association of Crohn's disease and ulcerative colitis with haplotypes of the MLH1 gene in Italian inflammatory bowel disease patientsV Annese, A Piepoli, A Andriulli, et al.
Pageof 25