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G Gimelli

Showing results (11-20 of 64) with videos related to

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European Journal of Medical Genetics|June 15, 2007
A large analphoid invdup(3)(q22.3qter) marker chromosome characterized by array-CGH in a child with malformations, mental retardation, ambiguous genitalia and Blaschko's linesG Gimelli, R Giorda, S Beri, et al.
Chromosoma|September 28, 2000
CENP-G in neocentromeres and inactive centromeresG Gimelli, O Zuffardi, S Giglio, et al.
Acta Cardiologica|July 21, 2000
Primary versus rescue percutaneous coronary intervention in patients with acute myocardial infarctionG Gimelli, A Kalra, M S Sabatine, et al.
Human Genetics|December 15, 1976
"Jumping" satellites in three generations: a warning for paternity tests and prenatal diagnosisG Gimelli, E Porro, F Santi, et al.
Journal of Medical Genetics|May 1, 1993
ICF syndrome with variable expression in sibsG Gimelli, P Varone, A Pezzolo, et al.
Prenatal Diagnosis|January 1, 1983
Prenatal diagnosis, fetal pathology and cytogenetic analysis of a 46,XX/47,XX, + 15 mosaicG Gimelli, C Cuoco, E Porro, et al.
Prenatal Diagnosis|August 1, 1990
Prenatal diagnosis of a partial 8p trisomyA Pezzolo, M P Bicocchi, C Zampatti, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|March 1, 1996
[18q syndrome with deficiency of myelin basic protein (MBP)]A Iester, S Vignola, L Callegarini, et al.
Prenatal Diagnosis|November 1, 1987
False-positive and false-negative findings on chorionic villus samplingG Simoni, M Fraccaro, G Gimelli, et al.
Human Genetics|February 1, 1994
Definitive assignment of the growth hormone-releasing factor gene to 20q11.2A Pezzolo, G Gimelli, M Sposito, et al.
Pageof 7

Showing results (11-20 of 64) with videos related to

Sort By:
Pageof 7
European Journal of Medical Genetics|June 15, 2007
A large analphoid invdup(3)(q22.3qter) marker chromosome characterized by array-CGH in a child with malformations, mental retardation, ambiguous genitalia and Blaschko's linesG Gimelli, R Giorda, S Beri, et al.
Chromosoma|September 28, 2000
CENP-G in neocentromeres and inactive centromeresG Gimelli, O Zuffardi, S Giglio, et al.
Acta Cardiologica|July 21, 2000
Primary versus rescue percutaneous coronary intervention in patients with acute myocardial infarctionG Gimelli, A Kalra, M S Sabatine, et al.
Human Genetics|December 15, 1976
"Jumping" satellites in three generations: a warning for paternity tests and prenatal diagnosisG Gimelli, E Porro, F Santi, et al.
Journal of Medical Genetics|May 1, 1993
ICF syndrome with variable expression in sibsG Gimelli, P Varone, A Pezzolo, et al.
Prenatal Diagnosis|January 1, 1983
Prenatal diagnosis, fetal pathology and cytogenetic analysis of a 46,XX/47,XX, + 15 mosaicG Gimelli, C Cuoco, E Porro, et al.
Prenatal Diagnosis|August 1, 1990
Prenatal diagnosis of a partial 8p trisomyA Pezzolo, M P Bicocchi, C Zampatti, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|March 1, 1996
[18q syndrome with deficiency of myelin basic protein (MBP)]A Iester, S Vignola, L Callegarini, et al.
Prenatal Diagnosis|November 1, 1987
False-positive and false-negative findings on chorionic villus samplingG Simoni, M Fraccaro, G Gimelli, et al.
Human Genetics|February 1, 1994
Definitive assignment of the growth hormone-releasing factor gene to 20q11.2A Pezzolo, G Gimelli, M Sposito, et al.
Pageof 7