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A Selicorni

Showing results (1-10 of 55) with videos related to

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American Journal of Medical Genetics|December 5, 2000
Malpuech syndrome: a possible relationship with the Wolf-Hirschhorn/Pitt-Roger-Danks phenotypeA Selicorni, F Faravelli
Minerva Pediatrica|October 20, 2007
[Follow-up of the neonate with malformation syndrome]L Memo, A Selicorni, G Zampino
American Journal of Medical Genetics|December 1, 1990
"C" trigonocephaly syndrome: two additional casesG Camera, G Serra, A Selicorni
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|May 1, 1993
[Syndromes in outpatient experience]F Lalatta, A Selicorni, V Briscioli
Journal of Intellectual Disability Research : JIDR|September 12, 2007
The behavioural phenotype of Cornelia de Lange Syndrome: a study of 56 individualsE Basile, L Villa, A Selicorni, et al.
American Journal of Medical Genetics|July 31, 1995
Kaufman oculocerebrofacial syndrome in a girl of 15 yearsV Briscioli, S Manoukian, A Selicorni, et al.
American Journal of Medical Genetics. Part A|June 5, 2003
Gastroesophageal reflux and Cornelia de Lange syndrome: typical and atypical symptomsS Luzzani, F Macchini, A Valadè, et al.
American Journal of Medical Genetics|March 3, 1997
Genotype-phenotype correlation in two sets of monozygotic twins with Williams syndromeP Castorina, A Selicorni, F Bedeschi, et al.
Clinical Dysmorphology|April 20, 2001
Brachyphalangy, feet polydactyly, absent/hypoplastic tibiae: a further case and review of main diagnostic findingsF Faravelli, M Di Rocco, G Stella, et al.
Journal of Medical Genetics|July 5, 2003
Unusual cognitive and behavioural profile in a Williams syndrome patient with atypical 7q11.23 deletionC Gagliardi, M C Bonaglia, A Selicorni, et al.
Pageof 6

Showing results (1-10 of 55) with videos related to

Sort By:
Pageof 6
American Journal of Medical Genetics|December 5, 2000
Malpuech syndrome: a possible relationship with the Wolf-Hirschhorn/Pitt-Roger-Danks phenotypeA Selicorni, F Faravelli
Minerva Pediatrica|October 20, 2007
[Follow-up of the neonate with malformation syndrome]L Memo, A Selicorni, G Zampino
American Journal of Medical Genetics|December 1, 1990
"C" trigonocephaly syndrome: two additional casesG Camera, G Serra, A Selicorni
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|May 1, 1993
[Syndromes in outpatient experience]F Lalatta, A Selicorni, V Briscioli
Journal of Intellectual Disability Research : JIDR|September 12, 2007
The behavioural phenotype of Cornelia de Lange Syndrome: a study of 56 individualsE Basile, L Villa, A Selicorni, et al.
American Journal of Medical Genetics|July 31, 1995
Kaufman oculocerebrofacial syndrome in a girl of 15 yearsV Briscioli, S Manoukian, A Selicorni, et al.
American Journal of Medical Genetics. Part A|June 5, 2003
Gastroesophageal reflux and Cornelia de Lange syndrome: typical and atypical symptomsS Luzzani, F Macchini, A Valadè, et al.
American Journal of Medical Genetics|March 3, 1997
Genotype-phenotype correlation in two sets of monozygotic twins with Williams syndromeP Castorina, A Selicorni, F Bedeschi, et al.
Clinical Dysmorphology|April 20, 2001
Brachyphalangy, feet polydactyly, absent/hypoplastic tibiae: a further case and review of main diagnostic findingsF Faravelli, M Di Rocco, G Stella, et al.
Journal of Medical Genetics|July 5, 2003
Unusual cognitive and behavioural profile in a Williams syndrome patient with atypical 7q11.23 deletionC Gagliardi, M C Bonaglia, A Selicorni, et al.
Pageof 6