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P Franceschini

Showing results (111-120 of 130) with videos related to

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Clinical Genetics|December 1, 1987
Postmortem Menkes diagnosis from carrier testing of female relativesT Tønnesen, M Silengo, A M Gerdes, et al.
American Journal of Medical Genetics|December 18, 1998
Long first metacarpal in monozygotic twins with probable Baller-Gerold syndromeP Franceschini, D Licata, A Guala, et al.
Prenatal Diagnosis|January 12, 2002
Prenatal diagnosis of kyphomelic dysplasiaA Guala, E Biroli, P Bassini, et al.
American Journal of Medical Genetics. Part A|September 5, 2003
Gershoni-Baruch syndrome: report of a new family confirming autosomal recessive inheritanceP Franceschini, A Guala, D Licata, et al.
Pediatric Radiology|January 1, 1986
Distinctive skeletal dysplasia in Cockayne syndromeM Cirillo Silengo, P Franceschini, R Bianco, et al.
Clinical Genetics|July 1, 1988
X/Y translocation in a family with X-linked ichthyosis, chondrodysplasia punctata, and mental retardation: DNA analysis reveals deletion of the steroid sulphatase gene and translocation of its Y pseudogeneA Ballabio, G Parenti, R Carrozzo, et al.
Panminerva Medica|December 1, 1995
Pre-B acute lymphoblastic leukemia in a patient with partial lipodystrophy and acanthosis nigricansP Franceschini, E Barisone, F Signorile, et al.
American Journal of Medical Genetics|January 1, 1992
Kenny-Caffey syndrome in two sibs born to consanguineous parents: evidence for an autosomal recessive variantP Franceschini, A Testa, G Bogetti, et al.
Clinical Genetics|December 1, 1986
Asymmetric crying facies with microcephaly and mental retardation. An autosomal dominant syndrome with variable expressivityM C Silengo, G L Bell, M Biagioli, et al.
AIDS (London, England)|September 1, 1991
HIV-1 seroprevalence in patients presenting with sexually transmitted disease (STD): results from six Parisian STD clinicsL Meyer, A Cavelier, M Bemhardt, et al.
Pageof 13

Showing results (111-120 of 130) with videos related to

Sort By:
Pageof 13
Clinical Genetics|December 1, 1987
Postmortem Menkes diagnosis from carrier testing of female relativesT Tønnesen, M Silengo, A M Gerdes, et al.
American Journal of Medical Genetics|December 18, 1998
Long first metacarpal in monozygotic twins with probable Baller-Gerold syndromeP Franceschini, D Licata, A Guala, et al.
Prenatal Diagnosis|January 12, 2002
Prenatal diagnosis of kyphomelic dysplasiaA Guala, E Biroli, P Bassini, et al.
American Journal of Medical Genetics. Part A|September 5, 2003
Gershoni-Baruch syndrome: report of a new family confirming autosomal recessive inheritanceP Franceschini, A Guala, D Licata, et al.
Pediatric Radiology|January 1, 1986
Distinctive skeletal dysplasia in Cockayne syndromeM Cirillo Silengo, P Franceschini, R Bianco, et al.
Clinical Genetics|July 1, 1988
X/Y translocation in a family with X-linked ichthyosis, chondrodysplasia punctata, and mental retardation: DNA analysis reveals deletion of the steroid sulphatase gene and translocation of its Y pseudogeneA Ballabio, G Parenti, R Carrozzo, et al.
Panminerva Medica|December 1, 1995
Pre-B acute lymphoblastic leukemia in a patient with partial lipodystrophy and acanthosis nigricansP Franceschini, E Barisone, F Signorile, et al.
American Journal of Medical Genetics|January 1, 1992
Kenny-Caffey syndrome in two sibs born to consanguineous parents: evidence for an autosomal recessive variantP Franceschini, A Testa, G Bogetti, et al.
Clinical Genetics|December 1, 1986
Asymmetric crying facies with microcephaly and mental retardation. An autosomal dominant syndrome with variable expressivityM C Silengo, G L Bell, M Biagioli, et al.
AIDS (London, England)|September 1, 1991
HIV-1 seroprevalence in patients presenting with sexually transmitted disease (STD): results from six Parisian STD clinicsL Meyer, A Cavelier, M Bemhardt, et al.
Pageof 13