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P Balestrazzi

Showing results (11-20 of 43) with videos related to

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Neurofibromatosis|January 1, 1989
Periaqueductal gliosis causing hydrocephalus in a patient with neurofibromatosis type 1P Balestrazzi, S de Gressi, A Donadio, et al.
Human Genetics|June 19, 1979
Partial trisomy 16q resulting from maternal translocationP Balestrazzi, G Giovannelli, L Landucci Rubini, et al.
Journal of Medical Genetics|October 1, 1983
Tetrasomy 9p confirmed by GALTP Balestrazzi, G Croci, C Frassi, et al.
Clinical Genetics|September 1, 1983
Familial pericentric inversion of chromosome 9, INV(9)(p22q32) with recurrent duplication-deletionJ F Mattei, M G Mattei, P Balestrazzi, et al.
Acta Haematologica|January 1, 1977
Cytogenetic studies in acute leukaemias. Prognostic implications of chromosome imbalancesG Alimena, L Annino, P Balestrazzi, et al.
L'Ateneo Parmense. Acta Bio-Medica : Organo Della Societa Di Medicina E Scienze Naturali Di Parma|January 1, 1980
[Mental retardation and sexual development in chromosomal syndrome (author's transl)]P Balestrazzi, S Bernasconi, F C Medioli, et al.
Human Genetics|January 1, 1983
Franceschetti syndrome in a child with a de novo balanced translocation (5;13)(q11;p11) and significant decrease of hexosaminidase BP Balestrazzi, M A Baeteman, M G Mattei, et al.
Journal of Endocrinological Investigation|September 1, 1993
The National Register of infants with congenital hypothyroidism detected by neonatal screening in ItalyM Sorcini, P Balestrazzi, M E Grandolfo, et al.
Pathologica|May 1, 1979
[Pathology of chromosome 16]P Balestrazzi, G Giovannelli, L Landucci, et al.
Journal of Human Hypertension|May 1, 1994
Hypertension in children with neurofibromatosisR Virdis, P Balestrazzi, M Zampolli, et al.
Pageof 5

Showing results (11-20 of 43) with videos related to

Sort By:
Pageof 5
Neurofibromatosis|January 1, 1989
Periaqueductal gliosis causing hydrocephalus in a patient with neurofibromatosis type 1P Balestrazzi, S de Gressi, A Donadio, et al.
Human Genetics|June 19, 1979
Partial trisomy 16q resulting from maternal translocationP Balestrazzi, G Giovannelli, L Landucci Rubini, et al.
Journal of Medical Genetics|October 1, 1983
Tetrasomy 9p confirmed by GALTP Balestrazzi, G Croci, C Frassi, et al.
Clinical Genetics|September 1, 1983
Familial pericentric inversion of chromosome 9, INV(9)(p22q32) with recurrent duplication-deletionJ F Mattei, M G Mattei, P Balestrazzi, et al.
Acta Haematologica|January 1, 1977
Cytogenetic studies in acute leukaemias. Prognostic implications of chromosome imbalancesG Alimena, L Annino, P Balestrazzi, et al.
L'Ateneo Parmense. Acta Bio-Medica : Organo Della Societa Di Medicina E Scienze Naturali Di Parma|January 1, 1980
[Mental retardation and sexual development in chromosomal syndrome (author's transl)]P Balestrazzi, S Bernasconi, F C Medioli, et al.
Human Genetics|January 1, 1983
Franceschetti syndrome in a child with a de novo balanced translocation (5;13)(q11;p11) and significant decrease of hexosaminidase BP Balestrazzi, M A Baeteman, M G Mattei, et al.
Journal of Endocrinological Investigation|September 1, 1993
The National Register of infants with congenital hypothyroidism detected by neonatal screening in ItalyM Sorcini, P Balestrazzi, M E Grandolfo, et al.
Pathologica|May 1, 1979
[Pathology of chromosome 16]P Balestrazzi, G Giovannelli, L Landucci, et al.
Journal of Human Hypertension|May 1, 1994
Hypertension in children with neurofibromatosisR Virdis, P Balestrazzi, M Zampolli, et al.
Pageof 5