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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 lines
G Gimelli, R Giorda, S Beri, et al.
Chromosoma
|
September 28, 2000
CENP-G in neocentromeres and inactive centromeres
G Gimelli, O Zuffardi, S Giglio, et al.
Acta Cardiologica
|
July 21, 2000
Primary versus rescue percutaneous coronary intervention in patients with acute myocardial infarction
G 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 diagnosis
G Gimelli, E Porro, F Santi, et al.
Journal of Medical Genetics
|
May 1, 1993
ICF syndrome with variable expression in sibs
G 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 mosaic
G Gimelli, C Cuoco, E Porro, et al.
Prenatal Diagnosis
|
August 1, 1990
Prenatal diagnosis of a partial 8p trisomy
A 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 sampling
G Simoni, M Fraccaro, G Gimelli, et al.
Human Genetics
|
February 1, 1994
Definitive assignment of the growth hormone-releasing factor gene to 20q11.2
A Pezzolo, G Gimelli, M Sposito, et al.
Page
of 7
Search research articles
Search
Showing results (11-20 of 64) with videos related to
Sort By:
Page
of 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 lines
G Gimelli, R Giorda, S Beri, et al.
Chromosoma
|
September 28, 2000
CENP-G in neocentromeres and inactive centromeres
G Gimelli, O Zuffardi, S Giglio, et al.
Acta Cardiologica
|
July 21, 2000
Primary versus rescue percutaneous coronary intervention in patients with acute myocardial infarction
G 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 diagnosis
G Gimelli, E Porro, F Santi, et al.
Journal of Medical Genetics
|
May 1, 1993
ICF syndrome with variable expression in sibs
G 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 mosaic
G Gimelli, C Cuoco, E Porro, et al.
Prenatal Diagnosis
|
August 1, 1990
Prenatal diagnosis of a partial 8p trisomy
A 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 sampling
G Simoni, M Fraccaro, G Gimelli, et al.
Human Genetics
|
February 1, 1994
Definitive assignment of the growth hormone-releasing factor gene to 20q11.2
A Pezzolo, G Gimelli, M Sposito, et al.
Page
of 7