Lista de obras -

A computational model of dysfunctional facial encoding in congenital prosopagnosia

artículo científico publicado en 2011

A family at risk: congenital prosopagnosia, poor face recognition and visuoperceptual deficits within one family

artículo científico publicado en 2014

A novel TACSTD2 gene mutation in a Turkish family with a gelatinous drop-like corneal dystrophy

artículo científico publicado en 2006

Clinical utility gene card for: Ehlers-Danlos syndrome types I-VII and variants - update 2012

artículo científico publicado en 2012

Clinical utility gene card for: Ehlers-Danlos syndrome types I-VII.

artículo científico publicado en 2010

Congenital prosopagnosia--a common hereditary cognitive dysfunction in humans

artículo científico publicado en 2008

Corrigendum: Do congenital prosopagnosia and the other-race effect affect the same face recognition mechanisms?

artículo científico publicado en 2015

Deficits in long-term recognition memory reveal dissociated subtypes in congenital prosopagnosia

artículo científico publicado en 2011

Face Perception and Test Reliabilities in Congenital Prosopagnosia in Seven Tests

artículo científico publicado en 2016

First report of prevalence of non-syndromic hereditary prosopagnosia (HPA).

artículo científico publicado en 2006

Galactose uncovers face recognition and mental images in congenital prosopagnosia: the first case report

artículo científico publicado en 2013

Gaze behaviour in hereditary prosopagnosia

artículo científico publicado en 2006

Genotype-phenotype correlations in Down syndrome identified by array CGH in 30 cases of partial trisomy and partial monosomy chromosome 21

artículo científico publicado en 2008

Hereditary prosopagnosia (HPA): the first report outside the Caucasian population

artículo científico publicado en 2006

Hereditary prosopagnosia: the first case series

artículo científico publicado en 2007

Mild phenotype in two unrelated patients with a partial deletion of 21q22.2-q22.3 defined by FISH and molecular studies

artículo científico publicado en 2004

Multicolor karyotyping in acute myeloid leukemia

artículo científico publicado en 2003

Novel der(1)t(1;19) in two patients with myeloid neoplasias

artículo científico publicado en 2002

Prevalence of hereditary prosopagnosia (HPA) in Hong Kong Chinese population

scientific article published on 01 November 2008

Situs ambiguus in a female fetus with balanced (X;21) translocation--evidence for functional nullisomy of the ZIC3 gene?

artículo científico publicado en 2005

Skeletal dysplasia in a consanguineous clan from the island of Nias/Indonesia is caused by a novel mutation in B3GAT3

scientific journal article

Sorting chromosomes as a software-based exercise ⬇️

artículo científico publicado el 1 de noviembre de 2010

Spectrum of skeletal abnormalities in a complex malformation syndrome with "cutis tricolor" (Ruggieri-Happle syndrome)

artículo científico publicado en 2011

The early time course of compensatory face processing in congenital prosopagnosia

artículo científico publicado en 2010

Unexpected island effects at an extreme: reduced Y chromosome and mitochondrial DNA diversity in Nias

artículo científico publicado en 2010

Lista de obras de

A computational model of dysfunctional facial encoding in congenital prosopagnosia

A family at risk: congenital prosopagnosia, poor face recognition and visuoperceptual deficits within one family

A novel TACSTD2 gene mutation in a Turkish family with a gelatinous drop-like corneal dystrophy

Clinical utility gene card for: Ehlers-Danlos syndrome types I-VII and variants - update 2012

Clinical utility gene card for: Ehlers-Danlos syndrome types I-VII.

Congenital prosopagnosia--a common hereditary cognitive dysfunction in humans

Corrigendum: Do congenital prosopagnosia and the other-race effect affect the same face recognition mechanisms?

Deficits in long-term recognition memory reveal dissociated subtypes in congenital prosopagnosia

Face Perception and Test Reliabilities in Congenital Prosopagnosia in Seven Tests

First report of prevalence of non-syndromic hereditary prosopagnosia (HPA).

Galactose uncovers face recognition and mental images in congenital prosopagnosia: the first case report

Gaze behaviour in hereditary prosopagnosia

Genotype-phenotype correlations in Down syndrome identified by array CGH in 30 cases of partial trisomy and partial monosomy chromosome 21

Hereditary prosopagnosia (HPA): the first report outside the Caucasian population

Hereditary prosopagnosia: the first case series

Mild phenotype in two unrelated patients with a partial deletion of 21q22.2-q22.3 defined by FISH and molecular studies

Multicolor karyotyping in acute myeloid leukemia

Novel der(1)t(1;19) in two patients with myeloid neoplasias

Prevalence of hereditary prosopagnosia (HPA) in Hong Kong Chinese population

Situs ambiguus in a female fetus with balanced (X;21) translocation--evidence for functional nullisomy of the ZIC3 gene?

Skeletal dysplasia in a consanguineous clan from the island of Nias/Indonesia is caused by a novel mutation in B3GAT3

Sorting chromosomes as a software-based exercise ⬇️

Spectrum of skeletal abnormalities in a complex malformation syndrome with "cutis tricolor" (Ruggieri-Happle syndrome)

The early time course of compensatory face processing in congenital prosopagnosia

Unexpected island effects at an extreme: reduced Y chromosome and mitochondrial DNA diversity in Nias