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M C Digilio

Showing results (21-30 of 130) with videos related to

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European Journal of Pediatrics|July 1, 1996
Search for 22q11 deletion in non-syndromic conotruncal cardiac defectsM C Digilio, B Marino, A Giannotti, et al.
Journal of Medical Genetics|May 1, 1996
Orocardiodigital syndrome: an oral-facial-digital type II variant associated with atrioventricular canalM C Digilio, B Marino, A Giannotti, et al.
Clinical Genetics|November 18, 2003
Postural anomaly of the head-neck-shoulder alignment in patients with deletion 22q11.2 (DiGeorge/velocardiofacial syndrome)M C Digilio, A Giannotti, B Dallapiccola, et al.
British Heart Journal|September 1, 1994
Familial atrioventricular septal defect: possible genetic mechanismM C Digilio, B Marino, A Giannotti, et al.
Journal of Medical Genetics|January 1, 1995
An autosomal recessive syndrome of cleft palate, cardiac defect, genital anomalies, and ectrodactyly (CCGE)A Giannotti, M C Digilio, R Mingarelli, et al.
Human Genetics|February 1, 1997
Noonan syndrome with cardiac left-sided obstructive lesionsM C Digilio, B Marino, A Giannotti, et al.
Cardiology in the Young|August 19, 2000
Deficiency of the infundibular septum in patients with interrupted aortic arch and del 22q11B Marino, M C Digilio, A Toscano, et al.
Human Genetics|August 1, 1995
Single atrium, atrioventricular canal/postaxial hexodactyly indicating Ellis-van Creveld syndromeM C Digilio, B Marino, A Giannotti, et al.
Journal of Medical Genetics|December 10, 1997
Conotruncal heart defect/microphthalmia syndrome: delineation of an autosomal recessive syndromeM C Digilio, B Marino, A Giannotti, et al.
Giornale Italiano Di Cardiologia|April 1, 1991
[Trisomy 18 associated with atrioventricular canal]M C Digilio, B Marino, A Giannotti, et al.
Pageof 13

Showing results (21-30 of 130) with videos related to

Sort By:
Pageof 13
European Journal of Pediatrics|July 1, 1996
Search for 22q11 deletion in non-syndromic conotruncal cardiac defectsM C Digilio, B Marino, A Giannotti, et al.
Journal of Medical Genetics|May 1, 1996
Orocardiodigital syndrome: an oral-facial-digital type II variant associated with atrioventricular canalM C Digilio, B Marino, A Giannotti, et al.
Clinical Genetics|November 18, 2003
Postural anomaly of the head-neck-shoulder alignment in patients with deletion 22q11.2 (DiGeorge/velocardiofacial syndrome)M C Digilio, A Giannotti, B Dallapiccola, et al.
British Heart Journal|September 1, 1994
Familial atrioventricular septal defect: possible genetic mechanismM C Digilio, B Marino, A Giannotti, et al.
Journal of Medical Genetics|January 1, 1995
An autosomal recessive syndrome of cleft palate, cardiac defect, genital anomalies, and ectrodactyly (CCGE)A Giannotti, M C Digilio, R Mingarelli, et al.
Human Genetics|February 1, 1997
Noonan syndrome with cardiac left-sided obstructive lesionsM C Digilio, B Marino, A Giannotti, et al.
Cardiology in the Young|August 19, 2000
Deficiency of the infundibular septum in patients with interrupted aortic arch and del 22q11B Marino, M C Digilio, A Toscano, et al.
Human Genetics|August 1, 1995
Single atrium, atrioventricular canal/postaxial hexodactyly indicating Ellis-van Creveld syndromeM C Digilio, B Marino, A Giannotti, et al.
Journal of Medical Genetics|December 10, 1997
Conotruncal heart defect/microphthalmia syndrome: delineation of an autosomal recessive syndromeM C Digilio, B Marino, A Giannotti, et al.
Giornale Italiano Di Cardiologia|April 1, 1991
[Trisomy 18 associated with atrioventricular canal]M C Digilio, B Marino, A Giannotti, et al.
Pageof 13