Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

M P Vardeu

Showing results (1-10 of 9) with videos related to

Pageof 1
Sort By:
American Journal of Medical Genetics|May 15, 1993
Monozygotic twinning and Wiedemann-Beckwith syndromeP Franceschini, A Guala, M P Vardeu, et al.
Clinical Dysmorphology|July 1, 1994
Rigid mask-like face, ear anomalies, deafness, preaxial polydactyly and toe malformations in a patient with normal intelligence: a new entity?P Franceschini, M P Vardeu, A Guala, et al.
American Journal of Medical Genetics|March 1, 1996
Ullrich-Turner phenotype with unusual manifestation in a patient with mosaicism 45,X/47,XX,+18P Franceschini, A Guala, P Camerano, et al.
American Journal of Medical Genetics|December 1, 1992
Possible relationship between ulnar-mammary syndrome and split hand with aplasia of the ulna syndromeP Franceschini, M P Vardeu, L Dalforno, et al.
American Journal of Medical Genetics|September 1, 1993
Lower lip pits and complete idiopathic precocious puberty in a patient with Kabuki make-up (Niikawa-Kuroki) syndromeP Franceschini, M P Vardeu, A Guala, et al.
American Journal of Medical Genetics|November 20, 1995
Short rib-dysplasia group (with/without polydactyly): report of a patient suggesting the existence of a continuous spectrumP Franceschini, A Guala, M P Vardeu, et al.
American Journal of Medical Genetics|May 15, 1993
Inguinal hernia and atrial septal defect in Tel Hashomer camptodactyly syndrome: report of a new case expanding the phenotypic spectrum of the diseaseP Franceschini, M P Vardeu, F Signorile, et al.
European Journal of Pediatrics|October 1, 1995
Variability of clinical and immunological phenotype in immunodeficiency-centromeric instability-facial anomalies syndrome. Report of two new patients and review of the literatureP Franceschini, S Martino, M Ciocchini, et al.
Minerva Pediatrica|October 1, 1996
The Williams syndrome: an Italian collaborative studyP Franceschini, A Guala, M P Vardeu, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
American Journal of Medical Genetics|May 15, 1993
Monozygotic twinning and Wiedemann-Beckwith syndromeP Franceschini, A Guala, M P Vardeu, et al.
Clinical Dysmorphology|July 1, 1994
Rigid mask-like face, ear anomalies, deafness, preaxial polydactyly and toe malformations in a patient with normal intelligence: a new entity?P Franceschini, M P Vardeu, A Guala, et al.
American Journal of Medical Genetics|March 1, 1996
Ullrich-Turner phenotype with unusual manifestation in a patient with mosaicism 45,X/47,XX,+18P Franceschini, A Guala, P Camerano, et al.
American Journal of Medical Genetics|December 1, 1992
Possible relationship between ulnar-mammary syndrome and split hand with aplasia of the ulna syndromeP Franceschini, M P Vardeu, L Dalforno, et al.
American Journal of Medical Genetics|September 1, 1993
Lower lip pits and complete idiopathic precocious puberty in a patient with Kabuki make-up (Niikawa-Kuroki) syndromeP Franceschini, M P Vardeu, A Guala, et al.
American Journal of Medical Genetics|November 20, 1995
Short rib-dysplasia group (with/without polydactyly): report of a patient suggesting the existence of a continuous spectrumP Franceschini, A Guala, M P Vardeu, et al.
American Journal of Medical Genetics|May 15, 1993
Inguinal hernia and atrial septal defect in Tel Hashomer camptodactyly syndrome: report of a new case expanding the phenotypic spectrum of the diseaseP Franceschini, M P Vardeu, F Signorile, et al.
European Journal of Pediatrics|October 1, 1995
Variability of clinical and immunological phenotype in immunodeficiency-centromeric instability-facial anomalies syndrome. Report of two new patients and review of the literatureP Franceschini, S Martino, M Ciocchini, et al.
Minerva Pediatrica|October 1, 1996
The Williams syndrome: an Italian collaborative studyP Franceschini, A Guala, M P Vardeu, et al.
Pageof 1