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L M Farah

Showing results (1-10 of 8) with videos related to

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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.
Revista Paulista De Medicina|January 1, 1989
[Balanced translocation 1;10(q41;q25): a report of a family]L M Farah, M Corbani, R Joffe, et al.
Humangenetik|August 25, 1975
Balanced homologous translocation t(22q22q) in a phenotypically normal woman with repeated spontaneous abortionsL M Farah, H R de Nazareth, M Dolnikoff, et al.
Human Genetics|June 10, 1977
Pure gonadal dysgenesis (type XX). Report on a family with four affected sibsH R Nazareth, L M Farah, A J Cunha, et al.
Revista Paulista De Medicina|March 1, 1987
[Alpha fetoprotein in the amniotic fluid of Brazilian pregnant women]E Costanzi, M E da Silva, L M Farah, et al.
American Journal of Medical Genetics|December 1, 1990
Terminal deletion 6p23: a case reportM H Kormann-Bortolotto, L M Farah, D Soares, et al.
Arquivos Brasileiros De Cardiologia|February 7, 2001
Recurrence of atrial septal defect in three generationsC Ferreira, L M Farah, R M Póvoa, et al.
American Journal of Human Genetics|February 1, 1994
A somatic origin of homologous Robertsonian translocations and isochromosomesW P Robinson, F Bernasconi, S Basaran, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
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.
Revista Paulista De Medicina|January 1, 1989
[Balanced translocation 1;10(q41;q25): a report of a family]L M Farah, M Corbani, R Joffe, et al.
Humangenetik|August 25, 1975
Balanced homologous translocation t(22q22q) in a phenotypically normal woman with repeated spontaneous abortionsL M Farah, H R de Nazareth, M Dolnikoff, et al.
Human Genetics|June 10, 1977
Pure gonadal dysgenesis (type XX). Report on a family with four affected sibsH R Nazareth, L M Farah, A J Cunha, et al.
Revista Paulista De Medicina|March 1, 1987
[Alpha fetoprotein in the amniotic fluid of Brazilian pregnant women]E Costanzi, M E da Silva, L M Farah, et al.
American Journal of Medical Genetics|December 1, 1990
Terminal deletion 6p23: a case reportM H Kormann-Bortolotto, L M Farah, D Soares, et al.
Arquivos Brasileiros De Cardiologia|February 7, 2001
Recurrence of atrial septal defect in three generationsC Ferreira, L M Farah, R M Póvoa, et al.
American Journal of Human Genetics|February 1, 1994
A somatic origin of homologous Robertsonian translocations and isochromosomesW P Robinson, F Bernasconi, S Basaran, et al.
Pageof 1