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Refinado por: autor: Bertola, D eliminar materia: Genética Médica eliminar Clinical Genetics eliminar
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Infantile sialic acid storage disease report of the first case in South America
Infantile sialic acid storage disease report of the first case in South America
Material Type:
Artículo 		Añadir a Mi Portal

Infantile sialic acid storage disease report of the first case in South America

C. Y. Utagawa S. M. M Sugayama; E. M Ribeiro; D. R Bertola; E. R Baba; M. G Burin; E Lewis; J. C Coelho; A. H Fensom; M. J Marques-Dias; Claudette Hajaj Gonzales; C. A Kim; R Giugliani

Clinical Genetics v. 55, n. 5, p. 386-387, 1999

1999

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2
Infantile sialic acid storage disease report of the first case in South America
Infantile sialic acid storage disease report of the first case in South America
Material Type:
Artículo 		Añadir a Mi Portal

Infantile sialic acid storage disease report of the first case in South America

C. Y. Utagawa S. M. M Sugayama; E. M Ribeiro; D. R Bertola; E. R Baba; M. G Burin; E Lewis; J. C Coelho; A. H Fensom; M. J Marques-Dias; Claudette Hajaj Gonzales; C. A Kim; R Giugliani

Clinical Genetics v. 55, n. 5, p. 386-387, 1999

1999

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3
Richieri-Costa-Pereira syndrome expanding its phenotypicand genotypic spectrum
Richieri-Costa-Pereira syndrome expanding its phenotypicand genotypic spectrum
Material Type:
Artículo 		Añadir a Mi Portal

Richieri-Costa-Pereira syndrome expanding its phenotypicand genotypic spectrum

D R Bertola G Hsia; L Alvizi; A Gardham; E. L Wakeling; G. L Yamamoto; R. S Honjo; L. A. N Oliveira; R. C. Di Francesco; B A Perez; C A Kim; Maria Rita Passos-Bueno

Clinical Genetics Hoboken online, p. 1-12, Feb. 2018

Hoboken 2018

Disponible en FM - Fac. Medicina    (OPI 26383 2018 )(Obténgalo)

4
Congenital limb deficiency genetic investigation of 44 individuals presenting mainly longitudinal defects in isolated or syndromic forms
Congenital limb deficiency genetic investigation of 44 individuals presenting mainly longitudinal defects in isolated or syndromic forms
Material Type:
Artículo 		Añadir a Mi Portal

Congenital limb deficiency genetic investigation of 44 individuals presenting mainly longitudinal defects in isolated or syndromic forms

Letícia Alves da Rocha Lucas Vieira Lacerda Pires; Guilherme Lopes Yamamoto; José Ricardo Magliocco Ceroni; Rachel Sayuri Honjo; Edgard de Novaes França Bisneto; Luiz Antônio Nunes Oliveira; Carla Rosenberg; Ana Cristina Victorino Krepischi; Maria Rita Passos-Bueno; Chong Ae Kim; Débora Romeo Bertola

Clinical Genetics Hoboken v. 100, n. 5, p. 615-623, 2021

Hoboken 2021

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por este autor/creador:

  1. Bertola, D
  2. Kim, C
  3. Baba, E
  4. Ribeiro, E
  5. Coelho, J

con este tema:

  1. Disostose Crâniofacial
  2. Genótipos
  3. Doenças Genéticas
  4. Malformações
  5. Fenótipos

  • Realización: ABCD-USP USP   Logos de Redes Sociales: Freepik

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