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D Brunoni

Showing results (1-10 of 37) with videos related to

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The Journal of Clinical Dysmorphology|January 1, 1984
Mesomelic dwarfism, skeletal abnormalities, and ectodermal dysplasiaD Brunoni
Annales De Genetique|January 1, 1987
Terminal deletion 1q43 in a newborn with hydrocephalusM C Ribeiro, D Brunoni
American Journal of Medical Genetics|December 15, 1991
Terminal deletion of chromosome 10q26 due to a paternal translocation [(7;10)(q36;q26)]C L Borovik, D Brunoni
Revista Paulista De Medicina|July 1, 1992
Perinatal factors associated with neural tube defects (anencephaly [correction of anancephaly], spina bifida and encephalocele)A J Ogata, L Camano, D Brunoni
Cardiology in the Young|May 14, 1999
Multiple rhabdomyomas in monozygotic twinsM M Zamith, D Brunoni, M Ebaid
Annales De Genetique|January 9, 1999
Partial Xp duplication due to a translocation t(X;15) in two male and two female patients: a familial case report and review of the literatureM I Melaragno, M A Ramos, D Brunoni
American Journal of Medical Genetics|December 1, 1987
Tibial aplasia-ectrodactyly as variant expression of the Gollop-Wolfgang complex: report of a Brazilian familyA Richieri-Costa, D Brunoni, J Laredo Filho, et al.
American Journal of Medical Genetics. Part A|November 26, 2009
Pseudoaminopterin syndrome: clinical report with new characteristicsN Sobreira, M Cernach, D Batista, et al.
The Journal of Clinical Dysmorphology|January 1, 1983
Syndrome identification case report 92: Hirschsprung megacolon, cleft lip and palate, mental retardation, and minor congenital malformationsD Brunoni, R Joffe, L M Farah, et al.
Cancer Genetics and Cytogenetics|June 1, 1988
Bilateral retinoblastoma associated with 13q-mosaicism. Possible manifestation of a germinal mutationM C Ribeiro, J A Andrade, C M Erwenne, et al.
Pageof 4

Showing results (1-10 of 37) with videos related to

Sort By:
Pageof 4
The Journal of Clinical Dysmorphology|January 1, 1984
Mesomelic dwarfism, skeletal abnormalities, and ectodermal dysplasiaD Brunoni
Annales De Genetique|January 1, 1987
Terminal deletion 1q43 in a newborn with hydrocephalusM C Ribeiro, D Brunoni
American Journal of Medical Genetics|December 15, 1991
Terminal deletion of chromosome 10q26 due to a paternal translocation [(7;10)(q36;q26)]C L Borovik, D Brunoni
Revista Paulista De Medicina|July 1, 1992
Perinatal factors associated with neural tube defects (anencephaly [correction of anancephaly], spina bifida and encephalocele)A J Ogata, L Camano, D Brunoni
Cardiology in the Young|May 14, 1999
Multiple rhabdomyomas in monozygotic twinsM M Zamith, D Brunoni, M Ebaid
Annales De Genetique|January 9, 1999
Partial Xp duplication due to a translocation t(X;15) in two male and two female patients: a familial case report and review of the literatureM I Melaragno, M A Ramos, D Brunoni
American Journal of Medical Genetics|December 1, 1987
Tibial aplasia-ectrodactyly as variant expression of the Gollop-Wolfgang complex: report of a Brazilian familyA Richieri-Costa, D Brunoni, J Laredo Filho, et al.
American Journal of Medical Genetics. Part A|November 26, 2009
Pseudoaminopterin syndrome: clinical report with new characteristicsN Sobreira, M Cernach, D Batista, et al.
The Journal of Clinical Dysmorphology|January 1, 1983
Syndrome identification case report 92: Hirschsprung megacolon, cleft lip and palate, mental retardation, and minor congenital malformationsD Brunoni, R Joffe, L M Farah, et al.
Cancer Genetics and Cytogenetics|June 1, 1988
Bilateral retinoblastoma associated with 13q-mosaicism. Possible manifestation of a germinal mutationM C Ribeiro, J A Andrade, C M Erwenne, et al.
Pageof 4