Jorge M Saraiva

Jorge M Saraiva

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Jorge M Saraiva

Jorge M Saraiva

Publications by authors named "Jorge M Saraiva"

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[Regarding the article "Adults with Down syndrome: characterization of a Portuguese sample"].

Authors:
Jorge M Saraiva

Acta Med Port 2014 May-Jun;27(3):281. Epub 2014 Jun 30.

Presidente da Direção. Colégio da Especialidade de Genética Médica. Ordem dos Médicos. Lisboa. Portugal Serviço de Genética Médica. Hospital Pediátrico. Centro Hospitalar e Universitário de Coimbra. Coimbra. Portugal. Clínica Universitária de Pediatria. Faculdade de Medicina. Universidade de Coimbra. Portugal.

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March 2016

Eating behaviors, body image, perfectionism, and self-esteem in a sample of Portuguese girls.

Braz J Psychiatry 2016 Feb;38(2):135-40

Universidade de Coimbra, Departamento de Psicologia, Faculdade de Medicina, Universidade de Coimbra, Departamento de Psicologia Faculdade de Medicina Universidade de Coimbra Portugal, Portugal, Departamento de Psicologia, Faculdade de Medicina, Universidade de Coimbra, Portugal.

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http://dx.doi.org/10.1590/1516-4446-2015-1723DOI Listing
February 2016

Oculo-auriculo-vertebral spectrum: a review of the literature and genetic update.

J Med Genet 2014 Oct 12;51(10):635-45. Epub 2014 Aug 12.

Faculty of Medical and Human Sciences, Manchester Centre for Genomic Medicine, Institute of Human Development, University of Manchester, Manchester, UK Central Manchester University Hospitals NHS Foundation Trust as part of Manchester Academic Health Science Centre (MAHSC), Manchester, UK.

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http://dx.doi.org/10.1136/jmedgenet-2014-102476DOI Listing
October 2014

Intellectual disability, unusual facial morphology and hand anomalies in sibs.

Am J Med Genet A 2013 Oct 15;161A(10):2401-6. Epub 2013 Aug 15.

Serviço de Genética Médica, Hospital Pediátrico, Centro Hospitalar e Universitário de Coimbra, Coimbra, Portugal; Clinical and Molecular Genetics Unit, UCL Institute of Child Health, London, UK.

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http://doi.wiley.com/10.1002/ajmg.a.36124
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http://dx.doi.org/10.1002/ajmg.a.36124DOI Listing
October 2013

Cryptic 7q36.2q36.3 deletion causes multiple congenital eye anomalies and craniofacial dysmorphism.

Am J Med Genet A 2013 Mar 7;161A(3):589-93. Epub 2013 Feb 7.

Centro Hospitalar e Universitário de Coimbra, Departamento Pediátrico, Serviço de Genética Medica, Coimbra, Portugal.

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http://dx.doi.org/10.1002/ajmg.a.35713DOI Listing
March 2013

An explanation for another familial case of Rett syndrome: maternal germline mosaicism.

Eur J Hum Genet 2007 Aug 18;15(8):902-4. Epub 2007 Apr 18.

Serviço de Genética Médica, Hospital Pediátrico de Coimbra, Coimbra, Portugal.

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http://dx.doi.org/10.1038/sj.ejhg.5201835DOI Listing
August 2007

Chloride channel 7 (CLCN7) gene mutations in intermediate autosomal recessive osteopetrosis.

Hum Genet 2003 Feb 7;112(2):186-9. Epub 2002 Nov 7.

Department of Medical Genetics and INSERM U393, Hôpital Necker Enfants Malades, 149 Rue de Sèvres, 75015 Paris, France.

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http://dx.doi.org/10.1007/s00439-002-0861-9DOI Listing
February 2003