alphabetic list of serialssubject list of serialsserials search author indexsubject index
Library collection

Database : article
Search on : STEINER, CARLOS EDUARDO [Author]
References found : 7 [refine]
Displaying: 1 .. 7   in format [ISO 690]
Curriculum: Lattes

page 1 of 1

   1 / 7
select
to print
 Nogueira, Roberto José Negrão et al. Anthropometric and body-mass composition suggests an intrinsic feature in Williams-Beuren syndrome. Rev. Assoc. Med. Bras., Dec 2011, vol.57, no.6, p.681-685. ISSN 0104-4230

   2 / 7
select
to print
 Steiner, Carlos Eduardo, Cintra, Maria Letícia and Marques-de-Faria, Antonia Paula Cutis laxa with growth and developmental delay, wrinkly skin syndrome and gerodermia osteodysplastica: a report of two unrelated patients and a literature review. Genet. Mol. Biol., 2005, vol.28, no.2, p.181-190. ISSN 1415-4757
    · abstract in english    · text in english

   3 / 7
select
to print
 Oliveira, Gisele Viana de et al. Deafness, palmoplantar hyperkeratosis, and knuckle pads with male-to-male transmission: Bart-Pumphrey syndrome. Genet. Mol. Biol., 2003, vol.26, no.2, p.129-131. ISSN 1415-4757
    · abstract in english    · text in english

   4 / 7
select
to print
 Steiner, Carlos Eduardo et al. Genotype and natural history in unrelated individual with phenylketonuria and autistic behavior. Arq. Neuro-Psiquiatr., June 2007, vol.65, no.2A, p.202-205. ISSN 0004-282X

   5 / 7
select
to print
 Steiner, Carlos Eduardo, Guerreiro, Marilisa Mantovani and Marques-de-Faria, Antonia Paula Genetic and neurological evaluation in a sample of individuals with pervasive developmental disorders. Arq. Neuro-Psiquiatr., June 2003, vol.61, no.2A, p.176-180. ISSN 0004-282X

   6 / 7
select
to print
 Steiner, Carlos Eduardo et al. Laboratorial diagnosis of fragile-X syndrome: experience in a sample of individuals with pervasive developmental disorders. Arq. Neuro-Psiquiatr., Sept 2005, vol.63, no.3a, p.564-570. ISSN 0004-282X

   7 / 7
select
to print
 Rim, Priscila Hae Hyun et al. Ocular findings in Brazilian identical twins with Cohen syndrome: case report. Arq. Bras. Oftalmol., Dec 2009, vol.72, no.6, p.815-818. ISSN 0004-2749

page 1 of 1
   


Refine the search
  Database : article Advanced form   
Search for : Free form    Basic form

    Search in field  
1  
2
3
 
           



Search engine: iAH powered by WWWISIS

BIREME/PAHO/WHO - Latin American and Caribbean Center on Health Sciences Information