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Journal of Medical Genetics
|
March 1, 1997
Recurrence risk figures for isolated tetralogy of Fallot after screening for 22q11 microdeletion
M C Digilio, B Marino, A Giannotti, et al.
The American Journal of Cardiology
|
November 1, 1992
Prevalence of bilateral patent ductus arteriosus in patients with pulmonic valve atresia and asplenia syndrome
R Formigari, U Vairo, A de Zorzi, et al.
Cardiologia (Rome, Italy)
|
May 1, 1991
[Recent applications of informatics in postoperative intensive therapy in heart surgery]
M Cassese, R Chiavarelli, M Chiavarelli, et al.
American Journal of Physical Anthropology
|
April 1, 1989
Nutritional status of Efe pygmies and Lese horticulturists
W H Dietz, B Marino, N R Peacock, et al.
Cardiologia (Rome, Italy)
|
August 1, 1997
[Study of the coronary flow with high resolution transthoracic echocardiography and nondirectional Doppler]
P Voci, G Testa, G Plaustro, et al.
American Heart Journal
|
June 1, 1987
Echocardiographic identification of aortic atresia with ventricular septal defect, normal left ventricle and mitral valve
B Marino, S P Sanders, I A Parness, et al.
Genetic Counseling (Geneva, Switzerland)
|
April 7, 1999
Congenital heart defects in patients with DiGeorge/velocardiofacial syndrome and del22q11
B Marino, M C Digilio, A Toscano, et al.
The Journal of Pediatrics
|
December 10, 1999
Congenital heart diseases in children with Noonan syndrome: An expanded cardiac spectrum with high prevalence of atrioventricular canal
B Marino, M C Digilio, A Toscano, et al.
American Journal of Medical Genetics
|
February 7, 1998
Intrafamilial variability of Pfeiffer-type cardiocranial syndrome
M C Digilio, B Marino, U Borzaga, et al.
American Journal of Medical Genetics
|
November 15, 1994
Cayler cardiofacial syndrome and del 22q11: part of the CATCH22 phenotype
A Giannotti, M C Digilio, B Marino, et al.
Page
of 43
Search research articles
Search
Showing results (151-160 of 428) with videos related to
Sort By:
Page
of 43
Journal of Medical Genetics
|
March 1, 1997
Recurrence risk figures for isolated tetralogy of Fallot after screening for 22q11 microdeletion
M C Digilio, B Marino, A Giannotti, et al.
The American Journal of Cardiology
|
November 1, 1992
Prevalence of bilateral patent ductus arteriosus in patients with pulmonic valve atresia and asplenia syndrome
R Formigari, U Vairo, A de Zorzi, et al.
Cardiologia (Rome, Italy)
|
May 1, 1991
[Recent applications of informatics in postoperative intensive therapy in heart surgery]
M Cassese, R Chiavarelli, M Chiavarelli, et al.
American Journal of Physical Anthropology
|
April 1, 1989
Nutritional status of Efe pygmies and Lese horticulturists
W H Dietz, B Marino, N R Peacock, et al.
Cardiologia (Rome, Italy)
|
August 1, 1997
[Study of the coronary flow with high resolution transthoracic echocardiography and nondirectional Doppler]
P Voci, G Testa, G Plaustro, et al.
American Heart Journal
|
June 1, 1987
Echocardiographic identification of aortic atresia with ventricular septal defect, normal left ventricle and mitral valve
B Marino, S P Sanders, I A Parness, et al.
Genetic Counseling (Geneva, Switzerland)
|
April 7, 1999
Congenital heart defects in patients with DiGeorge/velocardiofacial syndrome and del22q11
B Marino, M C Digilio, A Toscano, et al.
The Journal of Pediatrics
|
December 10, 1999
Congenital heart diseases in children with Noonan syndrome: An expanded cardiac spectrum with high prevalence of atrioventricular canal
B Marino, M C Digilio, A Toscano, et al.
American Journal of Medical Genetics
|
February 7, 1998
Intrafamilial variability of Pfeiffer-type cardiocranial syndrome
M C Digilio, B Marino, U Borzaga, et al.
American Journal of Medical Genetics
|
November 15, 1994
Cayler cardiofacial syndrome and del 22q11: part of the CATCH22 phenotype
A Giannotti, M C Digilio, B Marino, et al.
Page
of 43