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P Franceschini

Showing results (61-70 of 130) with videos related to

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Clinical and Experimental Obstetrics & Gynecology|January 1, 1994
Low-risk endometrial hyperplasia: hysteroscopy and histologic evaluation after treatment with LH-RH analogueS Pace, M Figliolini, A Grassi, et al.
Minerva Pediatrica|January 31, 1981
[Rhizomelic type of chondrodysplasia punctata in 2 sisters. Evidence for hereditary transmission of a recessive autosomic type]C Fabris, D Licata, C Martano, et al.
Radiology|September 1, 1974
The autosomal recessive form of spondylocostal dysostosisP Franceschini, E Grassi, C Fabris, et al.
Pediatric Radiology|April 5, 1974
First rib hypoplasia in Patau's diseaseP Franceschini, C Fabris, G Bogetti, et al.
American Journal of Medical Genetics|April 5, 2000
Arterial tortuosity syndromeP Franceschini, A Guala, D Licata, et al.
Human Genetics|January 1, 1983
Interstitial deletion of the long arm of chromosome 3 in a patient with mental retardation and congenital anomaliesP Franceschini, M Cirillo Silengo, G Davi, et al.
Clinical Dysmorphology|January 29, 2000
Radioulnar synostosis and XYY syndromeP Franceschini, D Licata, A Guala, et al.
Pediatrie|March 1, 1974
[Usefulness of fluorescent substances in studies of normal and pathological Karyotype]P Franceschini, C Fabris, G Bogetti, et al.
Helvetica Paediatrica Acta|April 1, 1972
Blast cell proliferation in perinatal leukaemia with chromosomal translocation(Bq+; Dq-)A Ponzone, C De Sanctis, C Fabris, et al.
Minerva Pediatrica|June 9, 1972
[Value of the use of fluorescent substances in the study of normal and pathologic human karyotypes. I. Identification of the Y chromosome]P Franceschini, C Fabris, G Bogetti, et al.
Pageof 13

Showing results (61-70 of 130) with videos related to

Sort By:
Pageof 13
Clinical and Experimental Obstetrics & Gynecology|January 1, 1994
Low-risk endometrial hyperplasia: hysteroscopy and histologic evaluation after treatment with LH-RH analogueS Pace, M Figliolini, A Grassi, et al.
Minerva Pediatrica|January 31, 1981
[Rhizomelic type of chondrodysplasia punctata in 2 sisters. Evidence for hereditary transmission of a recessive autosomic type]C Fabris, D Licata, C Martano, et al.
Radiology|September 1, 1974
The autosomal recessive form of spondylocostal dysostosisP Franceschini, E Grassi, C Fabris, et al.
Pediatric Radiology|April 5, 1974
First rib hypoplasia in Patau's diseaseP Franceschini, C Fabris, G Bogetti, et al.
American Journal of Medical Genetics|April 5, 2000
Arterial tortuosity syndromeP Franceschini, A Guala, D Licata, et al.
Human Genetics|January 1, 1983
Interstitial deletion of the long arm of chromosome 3 in a patient with mental retardation and congenital anomaliesP Franceschini, M Cirillo Silengo, G Davi, et al.
Clinical Dysmorphology|January 29, 2000
Radioulnar synostosis and XYY syndromeP Franceschini, D Licata, A Guala, et al.
Pediatrie|March 1, 1974
[Usefulness of fluorescent substances in studies of normal and pathological Karyotype]P Franceschini, C Fabris, G Bogetti, et al.
Helvetica Paediatrica Acta|April 1, 1972
Blast cell proliferation in perinatal leukaemia with chromosomal translocation(Bq+; Dq-)A Ponzone, C De Sanctis, C Fabris, et al.
Minerva Pediatrica|June 9, 1972
[Value of the use of fluorescent substances in the study of normal and pathologic human karyotypes. I. Identification of the Y chromosome]P Franceschini, C Fabris, G Bogetti, et al.
Pageof 13