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List of works by Danilo Moretti-Ferreira

A genetic linkage study in Brazil identifies a new locus for persistent developmental stuttering on chromosome 10.

scientific article published on 24 March 2014

A rare non-Robertsonian translocation involving chromosomes 15 and 21.

scientific article

A study of the role of the FOXP2 and CNTNAP2 genes in persistent developmental stuttering.

scientific article

Assessment of clinical scoring systems for the diagnosis of Williams-Beuren syndrome.

scientific article published on 4 September 2013

Autism spectrum disorder in a girl with a de novo x;19 balanced translocation

scientific article

Características clínicas, comportamentais, cognitivas e comunicativa na síndrome Smith-Magenis

Cytogenetic Evidence of Involvement of Chromosome Regions 15q12 and 12q15 in Conditions with Associated Overgrowth

article

Diagnosis of Smith-Lemli-Opitz syndrome by ultraviolet spectrophotometry.

scientific article published on 16 September 2003

Differential diagnosis of Smith-Magenis syndrome: 1p36 deletion syndrome

scientific article published on 07 April 2011

Evaluation of the association between polymorphisms at the DRD2 locus and stuttering

scientific article published on 10 March 2011

Genomic strategy identifies a missense mutation in WD-repeat domain 65 (WDR65) in an individual with Van der Woude syndrome

scientific article published on 13 May 2011

Genética e linguagem na síndrome de Williams-Beuren: uma condição neuro-cognitiva peculiar

article

High dosage folic acid supplementation, oral cleft recurrence and fetal growth

scientific article published on 4 February 2013

Identity by descent and candidate gene mapping of Richieri-Costa and Pereira syndrome

article

Linguagem narrativa e fluência na síndrome de down: uma revisão

Metacarpophalangeal pattern profile in Marfan syndrome and Marfan-like patients

scientific article published on 01 October 1997

Oral cleft prevention program (OCPP).

scientific article

Oropharyngeal dysphagia and language delay in partial trisomy 9p: case report.

scientific article published on 22 September 2009

Perfil comunicativo de indivíduos com a síndrome de Williams-Beuren

Prevalence and nonrandom distribution of exonic mutations in interferon regulatory factor 6 in 307 families with Van der Woude syndrome and 37 families with popliteal pterygium syndrome

scientific article

Schilbach-Rott/blepharofacioskeletal syndrome in a Brazilian patient

article

Speech fluency profile in Williams-Beuren syndrome: a preliminary study

scientific article published on April 2009

Sulcus vocalis: evidence for autosomal dominant inheritance

article

X-chromosome inactivation patterns in monozygotic twins and sib pairs discordant for nonsyndromic cleft lip and/or palate

scientific article