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R Vivarelli

Showing results (11-20 of 26) with videos related to

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Bollettino Della Societa Italiana Di Biologia Sperimentale|April 1, 1992
[Correlations between karyotype and phenotype in structural and numerical abnormalities of chromosome 18]R Vivarelli, M Paolieri, C Anichini, et al.
Brain & Development|February 28, 2001
Pseudo-TORCH syndrome or Baraitser-Reardon syndrome: diagnostic criteriaR Vivarelli, S Grosso, M Cioni, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|December 1, 1993
Central nervous system imaging in reevaluation of patients with neurofibromatosis type 1P Balestri, L Calistri, R Vivarelli, et al.
Journal of Medical Genetics|October 1, 1989
Alternate centromere inactivation in a pseudodicentric (15;20)(pter;pter) associated with a progressive neurological disorderH Rivera, O Zuffardi, P Maraschio, et al.
Bollettino Della Societa Italiana Di Biologia Sperimentale|March 1, 1992
[Correlation of the clinical phenotype with a pericentric inversion of chromosome 9]R Scarinci, C Anichini, R Vivarelli, et al.
Minerva Anestesiologica|February 10, 1999
[Premedication with intranasal midazolam in children of various ages]R Vivarelli, F Zanotti, D Battaglia, et al.
Bollettino Della Societa Italiana Di Biologia Sperimentale|March 1, 1992
[Familial segregation of simple and complex chromosomal rearrangements]C Anichini, R Vivarelli, R Scarinci, et al.
Minerva Anestesiologica|June 1, 1990
[Low T3 syndrome (3,3',5-triiodothyronine) in relation to the extent of surgical trauma]A Guberti, R Vivarelli, S Tartari, et al.
Bollettino Della Societa Italiana Di Biologia Sperimentale|July 1, 1991
[Serum T3, T4, FT3, TSH and TBG in Turner's syndrome]C De Felice, C Anichini, R Mattei, et al.
American Journal of Medical Genetics|September 5, 2002
Familial Axenfeld-Rieger anomaly, cardiac malformations, and sensorineural hearing loss: a provisionally unique genetic syndrome?S Grosso, M A Farnetani, R Berardi, et al.
Pageof 3

Showing results (11-20 of 26) with videos related to

Sort By:
Pageof 3
Bollettino Della Societa Italiana Di Biologia Sperimentale|April 1, 1992
[Correlations between karyotype and phenotype in structural and numerical abnormalities of chromosome 18]R Vivarelli, M Paolieri, C Anichini, et al.
Brain & Development|February 28, 2001
Pseudo-TORCH syndrome or Baraitser-Reardon syndrome: diagnostic criteriaR Vivarelli, S Grosso, M Cioni, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|December 1, 1993
Central nervous system imaging in reevaluation of patients with neurofibromatosis type 1P Balestri, L Calistri, R Vivarelli, et al.
Journal of Medical Genetics|October 1, 1989
Alternate centromere inactivation in a pseudodicentric (15;20)(pter;pter) associated with a progressive neurological disorderH Rivera, O Zuffardi, P Maraschio, et al.
Bollettino Della Societa Italiana Di Biologia Sperimentale|March 1, 1992
[Correlation of the clinical phenotype with a pericentric inversion of chromosome 9]R Scarinci, C Anichini, R Vivarelli, et al.
Minerva Anestesiologica|February 10, 1999
[Premedication with intranasal midazolam in children of various ages]R Vivarelli, F Zanotti, D Battaglia, et al.
Bollettino Della Societa Italiana Di Biologia Sperimentale|March 1, 1992
[Familial segregation of simple and complex chromosomal rearrangements]C Anichini, R Vivarelli, R Scarinci, et al.
Minerva Anestesiologica|June 1, 1990
[Low T3 syndrome (3,3',5-triiodothyronine) in relation to the extent of surgical trauma]A Guberti, R Vivarelli, S Tartari, et al.
Bollettino Della Societa Italiana Di Biologia Sperimentale|July 1, 1991
[Serum T3, T4, FT3, TSH and TBG in Turner's syndrome]C De Felice, C Anichini, R Mattei, et al.
American Journal of Medical Genetics|September 5, 2002
Familial Axenfeld-Rieger anomaly, cardiac malformations, and sensorineural hearing loss: a provisionally unique genetic syndrome?S Grosso, M A Farnetani, R Berardi, et al.
Pageof 3