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P Franceschini

Showing results (91-100 of 130) with videos related to

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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.
Minerva Pediatrica|June 16, 1974
[Identification of the Y chromosome and its anomalies, using induced fluorescence]M Sandrucci, C Fabris, G Bogetti, et al.
Revue De Stomatologie Et De Chirurgie Maxillo-Faciale|January 1, 1980
[Rapidly progressing basal-cell naevi (author's transl)]R Bataille, J C Vigneul, C Brami, et al.
Minerva Pediatrica|June 15, 1981
[Trisomy 22: a clinical diagnosis]M Cirillo Silengo, G Davi, R Bianco, et al.
Pediatric Radiology|January 1, 1987
A new syndrome with ocular, skeletal and renal involvementM Cirillo Silengo, G Lopez Bell, M Biagioli, et al.
Annales De Genetique|June 1, 1975
A family with three sibs carrying trisomy 21F Nuzzo, M Stefanini, G Simoni, 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.
Pediatric Radiology|January 1, 1986
The Coffin-Siris syndrome in two siblingsP Franceschini, M Cirillo Silengo, R Bianco, 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.
Pageof 13

Showing results (91-100 of 130) with videos related to

Sort By:
Pageof 13
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.
Minerva Pediatrica|June 16, 1974
[Identification of the Y chromosome and its anomalies, using induced fluorescence]M Sandrucci, C Fabris, G Bogetti, et al.
Revue De Stomatologie Et De Chirurgie Maxillo-Faciale|January 1, 1980
[Rapidly progressing basal-cell naevi (author's transl)]R Bataille, J C Vigneul, C Brami, et al.
Minerva Pediatrica|June 15, 1981
[Trisomy 22: a clinical diagnosis]M Cirillo Silengo, G Davi, R Bianco, et al.
Pediatric Radiology|January 1, 1987
A new syndrome with ocular, skeletal and renal involvementM Cirillo Silengo, G Lopez Bell, M Biagioli, et al.
Annales De Genetique|June 1, 1975
A family with three sibs carrying trisomy 21F Nuzzo, M Stefanini, G Simoni, 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.
Pediatric Radiology|January 1, 1986
The Coffin-Siris syndrome in two siblingsP Franceschini, M Cirillo Silengo, R Bianco, 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.
Pageof 13