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M Priolo

Showing results (1-10 of 21) with videos related to

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Journal of Medical Genetics|September 8, 2001
Ectodermal dysplasias: a new clinical-genetic classificationM Priolo, C Laganà
Clinical Genetics|January 10, 2001
Ectodermal dysplasias: not only 'skin' deepM Priolo, M Silengo, M Lerone, et al.
Clinical Dysmorphology|January 29, 2000
New clinical findings in oculo-ectodermal syndromeM Silengo, M Lerone, M Seri, et al.
American Journal of Medical Genetics|January 24, 1998
Ectodermal abnormalities in Kabuki syndromeM Lerone, M Priolo, A Naselli, et al.
Dermatology (Basel, Switzerland)|February 22, 2000
Total anonychia congenita in a woman with normal intelligence: report of a further caseM Priolo, L Rosaia, M Seri, et al.
Journal of Medical Genetics|February 7, 2001
Molecular characterisation of a supernumerary ring chromosome in a patient with VATER associationR Cinti, M Priolo, M Lerone, et al.
Clinical Genetics|August 17, 2000
Pfeiffer syndrome type 2 associated with a single amino acid deletion in the FGFR2 geneM Priolo, M Lerone, M Baffico, et al.
Journal of Obstetrics and Gynaecology : the Journal of the Institute of Obstetrics and Gynaecology|July 8, 2008
Caesarean section on request: are there loco-regional factors influencing maternal choice? An Italian experienceA Mancuso, A De Vivo, G Fanara, et al.
Prenatal Diagnosis|October 20, 2000
Sonographic and molecular diagnosis of thanatophoric dysplasia type I at 18 weeks of gestationP De Biasio, F Prefumo, M Baffico, et al.
American Journal of Medical Genetics|October 21, 1999
Congenital hypoplastic anaemia in a patient with a new multiple congenital anomalies-mental retardation syndromeP G Mori, M Priolo, M Lerone, et al.
Pageof 3

Showing results (1-10 of 21) with videos related to

Sort By:
Pageof 3
Journal of Medical Genetics|September 8, 2001
Ectodermal dysplasias: a new clinical-genetic classificationM Priolo, C Laganà
Clinical Genetics|January 10, 2001
Ectodermal dysplasias: not only 'skin' deepM Priolo, M Silengo, M Lerone, et al.
Clinical Dysmorphology|January 29, 2000
New clinical findings in oculo-ectodermal syndromeM Silengo, M Lerone, M Seri, et al.
American Journal of Medical Genetics|January 24, 1998
Ectodermal abnormalities in Kabuki syndromeM Lerone, M Priolo, A Naselli, et al.
Dermatology (Basel, Switzerland)|February 22, 2000
Total anonychia congenita in a woman with normal intelligence: report of a further caseM Priolo, L Rosaia, M Seri, et al.
Journal of Medical Genetics|February 7, 2001
Molecular characterisation of a supernumerary ring chromosome in a patient with VATER associationR Cinti, M Priolo, M Lerone, et al.
Clinical Genetics|August 17, 2000
Pfeiffer syndrome type 2 associated with a single amino acid deletion in the FGFR2 geneM Priolo, M Lerone, M Baffico, et al.
Journal of Obstetrics and Gynaecology : the Journal of the Institute of Obstetrics and Gynaecology|July 8, 2008
Caesarean section on request: are there loco-regional factors influencing maternal choice? An Italian experienceA Mancuso, A De Vivo, G Fanara, et al.
Prenatal Diagnosis|October 20, 2000
Sonographic and molecular diagnosis of thanatophoric dysplasia type I at 18 weeks of gestationP De Biasio, F Prefumo, M Baffico, et al.
American Journal of Medical Genetics|October 21, 1999
Congenital hypoplastic anaemia in a patient with a new multiple congenital anomalies-mental retardation syndromeP G Mori, M Priolo, M Lerone, et al.
Pageof 3