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A Giannotti

Showing results (1-10 of 134) with videos related to

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La Clinica Terapeutica|October 31, 1981
[The use of kanendomycin in aerosol administration in chronic obstructive bronchopneumopathy]G Bottino, A Giannotti, E Costa
Human Genetics|May 1, 1988
Deletion 2q31.3----2q33.3: gene dosage effect of ribulose 5-phosphate 3-epimeraseB Dallapiccola, G Novelli, A Giannotti
Minerva Pediatrica|April 28, 2000
Langer-Giedion syndrome. A patient without mental retardation and a large 8q23.2-q24.22 deletionG Tiberio, M C Digilio, A Giannotti
Clinical Dysmorphology|January 29, 2000
Obesity and WAGR syndromeG Tiberio, M C Digilio, A Giannotti
Annales De Genetique|January 1, 1989
Digeorge anomaly associated with partial deletion of chromosome 22. Report of a case with X/22 translocation and review of the literatureB Dallapiccola, B Marino, A Giannotti, et al.
American Journal of Medical Genetics|August 1, 1989
Autosomal recessive form of whistling face syndrome in sibsB Dallapiccola, A Giannotti, A Lembo, et al.
Chest|January 1, 1991
Di George anomaly with atrioventricular canalB Marino, C Marcelletti, A Giannotti, et al.
American Journal of Medical Genetics|January 31, 1998
Familial recurrence of transposition of the great arteries and intact ventricular septumM C Digilio, B Marino, A Giannotti, et al.
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.
Pageof 14

Showing results (1-10 of 134) with videos related to

Sort By:
Pageof 14
La Clinica Terapeutica|October 31, 1981
[The use of kanendomycin in aerosol administration in chronic obstructive bronchopneumopathy]G Bottino, A Giannotti, E Costa
Human Genetics|May 1, 1988
Deletion 2q31.3----2q33.3: gene dosage effect of ribulose 5-phosphate 3-epimeraseB Dallapiccola, G Novelli, A Giannotti
Minerva Pediatrica|April 28, 2000
Langer-Giedion syndrome. A patient without mental retardation and a large 8q23.2-q24.22 deletionG Tiberio, M C Digilio, A Giannotti
Clinical Dysmorphology|January 29, 2000
Obesity and WAGR syndromeG Tiberio, M C Digilio, A Giannotti
Annales De Genetique|January 1, 1989
Digeorge anomaly associated with partial deletion of chromosome 22. Report of a case with X/22 translocation and review of the literatureB Dallapiccola, B Marino, A Giannotti, et al.
American Journal of Medical Genetics|August 1, 1989
Autosomal recessive form of whistling face syndrome in sibsB Dallapiccola, A Giannotti, A Lembo, et al.
Chest|January 1, 1991
Di George anomaly with atrioventricular canalB Marino, C Marcelletti, A Giannotti, et al.
American Journal of Medical Genetics|January 31, 1998
Familial recurrence of transposition of the great arteries and intact ventricular septumM C Digilio, B Marino, A Giannotti, et al.
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.
Pageof 14