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S M Sugayama

Showing results (1-10 of 9) with videos related to

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AJNR. American Journal of Neuroradiology|December 1, 2004
Malformation of cortical and vascular development in one family with parietal foramina determined by an ALX4 homeobox gene mutationMarcelo Valente, Kette D Valente, Sofia S M Sugayama, et al.
Revista Do Hospital Das Clinicas|May 2, 2000
Noonan syndrome: a clinical and genetic study of 31 patientsD R Bertola, S M Sugayama, L M Albano, et al.
Pediatric Dermatology|July 8, 2000
AEC syndrome and CHAND syndrome: further evidence of clinical overlapping in the ectodermal dysplasiasD R Bertola, C A Kim, S M Sugayama, et al.
Arquivos Brasileiros De Cardiologia|November 18, 2000
Cardiac findings in 31 patients with Noonan's syndromeD R Bertola, C A Kim, S M Sugayama, et al.
Revista Do Hospital Das Clinicas|October 8, 1999
Clinical and radiological aspects in Melnick-Needles syndromeL M Albano, C A Kim, V K Lee, et al.
Lancet (London, England)|June 10, 1998
Congenital abnormalities in Brazilian children associated with misoprostol misuse in first trimester of pregnancyC H Gonzalez, M J Marques-Dias, C A Kim, et al.
Revista Do Hospital Das Clinicas|January 10, 2002
Friedreich's ataxia: clinical and molecular study of 25 Brazilian casesL M Albano, M Zatz, C A Kim, et al.
Nature Genetics|January 4, 2001
Haploinsufficiency of the human homeobox gene ALX4 causes skull ossification defectsL A Mavrogiannis, I Antonopoulou, A Baxová, et al.
American Journal of Medical Genetics|February 24, 2001
Prenatal exposure to misoprostol and vascular disruption defects: a case-control studyF R Vargas, L Schuler-Faccini, D Brunoni, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
AJNR. American Journal of Neuroradiology|December 1, 2004
Malformation of cortical and vascular development in one family with parietal foramina determined by an ALX4 homeobox gene mutationMarcelo Valente, Kette D Valente, Sofia S M Sugayama, et al.
Revista Do Hospital Das Clinicas|May 2, 2000
Noonan syndrome: a clinical and genetic study of 31 patientsD R Bertola, S M Sugayama, L M Albano, et al.
Pediatric Dermatology|July 8, 2000
AEC syndrome and CHAND syndrome: further evidence of clinical overlapping in the ectodermal dysplasiasD R Bertola, C A Kim, S M Sugayama, et al.
Arquivos Brasileiros De Cardiologia|November 18, 2000
Cardiac findings in 31 patients with Noonan's syndromeD R Bertola, C A Kim, S M Sugayama, et al.
Revista Do Hospital Das Clinicas|October 8, 1999
Clinical and radiological aspects in Melnick-Needles syndromeL M Albano, C A Kim, V K Lee, et al.
Lancet (London, England)|June 10, 1998
Congenital abnormalities in Brazilian children associated with misoprostol misuse in first trimester of pregnancyC H Gonzalez, M J Marques-Dias, C A Kim, et al.
Revista Do Hospital Das Clinicas|January 10, 2002
Friedreich's ataxia: clinical and molecular study of 25 Brazilian casesL M Albano, M Zatz, C A Kim, et al.
Nature Genetics|January 4, 2001
Haploinsufficiency of the human homeobox gene ALX4 causes skull ossification defectsL A Mavrogiannis, I Antonopoulou, A Baxová, et al.
American Journal of Medical Genetics|February 24, 2001
Prenatal exposure to misoprostol and vascular disruption defects: a case-control studyF R Vargas, L Schuler-Faccini, D Brunoni, et al.
Pageof 1