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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.
Pediatric Cardiology
|
October 1, 1991
Turner's syndrome with atrioventricular canal
B Marino, M C Digilio, M Papa, et al.
The Journal of Pediatrics
|
April 1, 1997
Conotruncal heart defects and chromosome 22q11 microdeletion
M C Digilio, B Marino, A Giannotti, et al.
Minerva Pediatrica
|
January 1, 1992
[Partial deletion of the long arm of chromosome 17. Presentation of a clinical case]
A Giannotti, A Alessandri, A Reale, et al.
European Journal of Pediatrics
|
July 1, 1993
Discrete membranous subaortic stenosis in siblings
M C Digilio, A Giannotti, B Marino, et al.
Pediatric Cardiology
|
July 1, 1996
Partial atrioventricular canal with left-sided obstruction in patients with Noonan syndrome
B Marino, M C Digilio, M G Gagliardi, et al.
American Journal of Medical Genetics
|
September 20, 2000
Heterotaxy with left atrial isomerism in a patient with deletion 18p
M C Digilio, B Marino, A Giannotti, et al.
Teratology
|
April 25, 2000
Familial recurrence of nonsyndromic interrupted aortic arch and truncus arteriosus with atrioventricular canal
M C Digilio, B Marino, A M Musolino, et al.
The American Journal of Cardiology
|
June 15, 1996
Comparison of occurrence of genetic syndromes in ventricular septal defect with pulmonic stenosis (classic tetralogy of Fallot) versus ventricular septal defect with pulmonic atresia
M C Digilio, B Marino, S Grazioli, et al.
Pediatric Cardiology
|
March 15, 2002
Exercise testing and 24-hour ambulatory blood pressure monitoring in children with Williams syndrome
U Giordano, A Turchetta, A Giannotti, et al.
Page
of 13
Search research articles
Search
Showing results (51-60 of 130) with videos related to
Sort By:
Page
of 13
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.
Pediatric Cardiology
|
October 1, 1991
Turner's syndrome with atrioventricular canal
B Marino, M C Digilio, M Papa, et al.
The Journal of Pediatrics
|
April 1, 1997
Conotruncal heart defects and chromosome 22q11 microdeletion
M C Digilio, B Marino, A Giannotti, et al.
Minerva Pediatrica
|
January 1, 1992
[Partial deletion of the long arm of chromosome 17. Presentation of a clinical case]
A Giannotti, A Alessandri, A Reale, et al.
European Journal of Pediatrics
|
July 1, 1993
Discrete membranous subaortic stenosis in siblings
M C Digilio, A Giannotti, B Marino, et al.
Pediatric Cardiology
|
July 1, 1996
Partial atrioventricular canal with left-sided obstruction in patients with Noonan syndrome
B Marino, M C Digilio, M G Gagliardi, et al.
American Journal of Medical Genetics
|
September 20, 2000
Heterotaxy with left atrial isomerism in a patient with deletion 18p
M C Digilio, B Marino, A Giannotti, et al.
Teratology
|
April 25, 2000
Familial recurrence of nonsyndromic interrupted aortic arch and truncus arteriosus with atrioventricular canal
M C Digilio, B Marino, A M Musolino, et al.
The American Journal of Cardiology
|
June 15, 1996
Comparison of occurrence of genetic syndromes in ventricular septal defect with pulmonic stenosis (classic tetralogy of Fallot) versus ventricular septal defect with pulmonic atresia
M C Digilio, B Marino, S Grazioli, et al.
Pediatric Cardiology
|
March 15, 2002
Exercise testing and 24-hour ambulatory blood pressure monitoring in children with Williams syndrome
U Giordano, A Turchetta, A Giannotti, et al.
Page
of 13