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P Franceschini

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Human Genetics|January 1, 1983
Interstitial deletion of the long arm of chromosome 2 (q31q33) in a girl with multiple anomalies and mental retardationP Franceschini, M Cirillo Silengo, G Davi, et al.
Genetic Counseling (Geneva, Switzerland)|November 6, 2002
Filippi syndrome: a specific MCA/MR complex within the spectrum of so called "craniodigital syndromes". Report of an additional patient with a peculiar mpp and review of the literatureP Franceschini, D Licata, A Guala, et al.
American Journal of Medical Genetics|February 15, 2001
Peculiar facial appearance and generalized brachydactyly in a patient with congenital onychodysplasia of the index fingers (Iso-Kikuchi syndrome)P Franceschini, D Licata, A Guala, et al.
Minerva Pediatrica|March 3, 1973
[Value of the use of fluorescent dyes in the study of normal and pathological human karyotypes. II. Normal human karyotype]P Franceschini, C Fabris, G Bogetti, et al.
Minerva Pediatrica|October 20, 1971
[Congenital methemoglobulinemia of recessive type caused by DPNH-methemoglobin reductase deficiency. Description of a family]C Fabris, M T Norelli, G Ciriotti, et al.
Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine|June 1, 1986
Preparation of oxygen-15 butanol for positron tomographyM S Berridge, M P Franceschini, T J Tewson, et al.
Clinical Genetics|January 1, 1987
Triphalangeal thumb and brachy-ectrodactyly syndrome. Confirmation of autosomal dominant inheritanceM C Silengo, M Biagioli, G L Bell, et al.
Il Giornale Di Chirurgia|November 1, 1991
[Colonic stenosis due to a "microcarcinoma" of the ovary: a clinical note]A Brescia, L Giacomelli, H Hadjiamiri, et al.
Minerva Pediatrica|October 20, 1972
[Male pseudohermaphroditism. Importance and difficulties in the early assessment of the sex]P Franceschini, C Fabris, G Bogetti, et al.
Annales De Radiologie|May 1, 1974
[Skeletal alterations in Edwards' disease (trisomy 18 syndrome)]P Franceschini, C Fabris, A Ponzone, et al.
Pageof 13

Showing results (71-80 of 130) with videos related to

Sort By:
Pageof 13
Human Genetics|January 1, 1983
Interstitial deletion of the long arm of chromosome 2 (q31q33) in a girl with multiple anomalies and mental retardationP Franceschini, M Cirillo Silengo, G Davi, et al.
Genetic Counseling (Geneva, Switzerland)|November 6, 2002
Filippi syndrome: a specific MCA/MR complex within the spectrum of so called "craniodigital syndromes". Report of an additional patient with a peculiar mpp and review of the literatureP Franceschini, D Licata, A Guala, et al.
American Journal of Medical Genetics|February 15, 2001
Peculiar facial appearance and generalized brachydactyly in a patient with congenital onychodysplasia of the index fingers (Iso-Kikuchi syndrome)P Franceschini, D Licata, A Guala, et al.
Minerva Pediatrica|March 3, 1973
[Value of the use of fluorescent dyes in the study of normal and pathological human karyotypes. II. Normal human karyotype]P Franceschini, C Fabris, G Bogetti, et al.
Minerva Pediatrica|October 20, 1971
[Congenital methemoglobulinemia of recessive type caused by DPNH-methemoglobin reductase deficiency. Description of a family]C Fabris, M T Norelli, G Ciriotti, et al.
Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine|June 1, 1986
Preparation of oxygen-15 butanol for positron tomographyM S Berridge, M P Franceschini, T J Tewson, et al.
Clinical Genetics|January 1, 1987
Triphalangeal thumb and brachy-ectrodactyly syndrome. Confirmation of autosomal dominant inheritanceM C Silengo, M Biagioli, G L Bell, et al.
Il Giornale Di Chirurgia|November 1, 1991
[Colonic stenosis due to a "microcarcinoma" of the ovary: a clinical note]A Brescia, L Giacomelli, H Hadjiamiri, et al.
Minerva Pediatrica|October 20, 1972
[Male pseudohermaphroditism. Importance and difficulties in the early assessment of the sex]P Franceschini, C Fabris, G Bogetti, et al.
Annales De Radiologie|May 1, 1974
[Skeletal alterations in Edwards' disease (trisomy 18 syndrome)]P Franceschini, C Fabris, A Ponzone, et al.
Pageof 13