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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. Part A|April 23, 2004
Patterson-Lowry rhizomelic dysplasia: report of two new patientsPiergiorgio Franceschini, D Licata, A Guala, et al.Minerva Pediatrica|July 1, 1994
[Spasmus nutans. A re-emergent pathology?]A Guala, S Manieri, T Ghini, et al.American Journal of Medical Genetics|January 31, 1998
Esophageal atresia with distal tracheoesophageal fistula in a patient with fronto-metaphyseal dysplasiaP Franceschini, A Guala, D Licata, et al.American Journal of Medical Genetics|March 10, 2000
Macrocephaly-Cutis marmorata telangiectatica congenita without cutis marmorata?P Franceschini, D Licata, G Di Cara, et al.Genetic Counseling (Geneva, Switzerland)|May 23, 2002
A mentally retarded female with distinct facial dysmorphism, joint laxity, clinodactyly and abnormal dermatoglyphicsP Franceschini, A Guala, D Besana, 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.La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|August 23, 2006
[Sleeping in the supine position in the ASL 11 region of Piemonte. Assessment of the efficacy of a promotional campaign]A Guala, R Guarino, D Campra, et al.American Journal of Medical Genetics|October 23, 1997
Ring chromosome 13 with loss of the region D13S317-D13S285: phenotypic overlap with XK syndromeA Guala, C Dellavecchia, S Mannarino, et al.La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|March 1, 1991
[Hypophosphatasia: a family study]A Guala, P Tomà, M E Liverani, et al.Pageof 10