Franceschini, P.
525  Ergebnisse:
Personensuche X
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7

Gershoni–Baruch syndrome: Report of a new family confirming..:

Franceschini, P. ; Guala, A. ; Licata, D....
American Journal of Medical Genetics Part A.  122A (2003)  2 - p. 174-179 , 2003
 
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9

Reply to correspondence by Prais et al.—"COIF syndrome: The..:

Franceschini, P. ; Licata, D. ; Guala, A...
American Journal of Medical Genetics.  107 (2001)  2 - p. 180-180 , 2001
 
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10

Peculiar facial appearance and generalized brachydactyly in..:

Franceschini, P. ; Licata, D. ; Guala, A...
American Journal of Medical Genetics.  98 (2001)  4 - p. 330-335 , 2001
 
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11

Prenatal diagnosis of Nonne‐Milroy lymphedema:

Franceschini, P. ; Licata, D. ; Rapello, G....
Ultrasound in Obstetrics & Gynecology.  18 (2001)  2 - p. 182-183 , 2001
 
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12

Prenatal diagnosis of kyphomelic dysplasia:

Guala, A. ; Biroli, E. ; Bassini, P....
Prenatal Diagnosis.  21 (2001)  13 - p. 1146-1149 , 2001
 
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13

Synthesis of highly ethynylated mono and dinuclear Pt(II) t..:

Russo, M.V ; Lo Sterzo, C ; Franceschini, P..
Journal of Organometallic Chemistry.  619 (2001)  1-2 - p. 49-61 , 2001
 
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14

Macrocephaly-cutis marmorata telangiectatica congenita with..:

Franceschini, P. ; Licata, D. ; Di Cara, G....
American Journal of Medical Genetics.  90 (2000)  4 - p. 265-269 , 2000
 
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15

Radioulnar synostosis and XYY syndrome:

Franceschini, P. ; Licata, D. ; Guala, A...
Clinical Dysmorphology.  9 (2000)  1 - p. 77 , 2000
 
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