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A Guala

Showing results (81-90 of 100) with videos related to

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Panminerva Medica|December 1, 1995
Pre-B acute lymphoblastic leukemia in a patient with partial lipodystrophy and acanthosis nigricansP Franceschini, E Barisone, F Signorile, et al.
Pathologica|April 15, 2004
[Sex chromosome abnormality: report of three clinical cases of X pentasomy]E Biroli, C Ghimenti, I Ricci, et al.
American Journal of Medical Genetics|January 1, 1992
Kenny-Caffey syndrome in two sibs born to consanguineous parents: evidence for an autosomal recessive variantP Franceschini, A Testa, G Bogetti, et al.
Minerva Pediatrica|June 26, 2012
[The Cri du Chat syndrome: a study on the quality of care]P Cerruti Mainardi, M Spunton, V Arcuri, et al.
Minerva Pediatrica|February 21, 2013
Epistaxis in children under the age of two: possible marker of abuse/neglect? A retrospective study in North-Eastern Piedmont hospitalsL Boscardini, S Zanetta, G Ballardini, et al.
Journal of Medical Genetics|April 6, 2001
A novel mutation and novel features in Nijmegen breakage syndromeP Maraschio, C Danesino, A Antoccia, et al.
Cancer Genetics and Cytogenetics|August 25, 1999
Early onset of gastric carcinoma and constitutional deletion of 18pC Dellavecchia, A Guala, C Olivieri, et al.
Clinical Genetics|December 1, 1986
Asymmetric crying facies with microcephaly and mental retardation. An autosomal dominant syndrome with variable expressivityM C Silengo, G L Bell, M Biagioli, et al.
Minerva Pediatrica|July 1, 1992
[Celiac disease in Piedmont. An epidemiological-clinical study]N Ansaldi, D Dell'Olio, K Tavassoli, et al.
European Journal of Pediatrics|October 1, 1995
Variability of clinical and immunological phenotype in immunodeficiency-centromeric instability-facial anomalies syndrome. Report of two new patients and review of the literatureP Franceschini, S Martino, M Ciocchini, et al.
Pageof 10

Showing results (81-90 of 100) with videos related to

Sort By:
Pageof 10
Panminerva Medica|December 1, 1995
Pre-B acute lymphoblastic leukemia in a patient with partial lipodystrophy and acanthosis nigricansP Franceschini, E Barisone, F Signorile, et al.
Pathologica|April 15, 2004
[Sex chromosome abnormality: report of three clinical cases of X pentasomy]E Biroli, C Ghimenti, I Ricci, et al.
American Journal of Medical Genetics|January 1, 1992
Kenny-Caffey syndrome in two sibs born to consanguineous parents: evidence for an autosomal recessive variantP Franceschini, A Testa, G Bogetti, et al.
Minerva Pediatrica|June 26, 2012
[The Cri du Chat syndrome: a study on the quality of care]P Cerruti Mainardi, M Spunton, V Arcuri, et al.
Minerva Pediatrica|February 21, 2013
Epistaxis in children under the age of two: possible marker of abuse/neglect? A retrospective study in North-Eastern Piedmont hospitalsL Boscardini, S Zanetta, G Ballardini, et al.
Journal of Medical Genetics|April 6, 2001
A novel mutation and novel features in Nijmegen breakage syndromeP Maraschio, C Danesino, A Antoccia, et al.
Cancer Genetics and Cytogenetics|August 25, 1999
Early onset of gastric carcinoma and constitutional deletion of 18pC Dellavecchia, A Guala, C Olivieri, et al.
Clinical Genetics|December 1, 1986
Asymmetric crying facies with microcephaly and mental retardation. An autosomal dominant syndrome with variable expressivityM C Silengo, G L Bell, M Biagioli, et al.
Minerva Pediatrica|July 1, 1992
[Celiac disease in Piedmont. An epidemiological-clinical study]N Ansaldi, D Dell'Olio, K Tavassoli, et al.
European Journal of Pediatrics|October 1, 1995
Variability of clinical and immunological phenotype in immunodeficiency-centromeric instability-facial anomalies syndrome. Report of two new patients and review of the literatureP Franceschini, S Martino, M Ciocchini, et al.
Pageof 10