Lúcia Moraes

Cytogenetic and molecular studies of an X;21 translocation previously diagnosed as complete monosomy 21

Leila C.A. Cardoso, Lúcia Moraes, Maria Jesus E. Camilo et al. · European Journal of Medical Genetics · 2008 · 73 citations

Life Sciences, Genetics, Molecular Genetics +11

Severe phenotype in MPS II patients associated with a large deletion including contiguous genes

Ana Carolina Brusius‐Facchin, Carolina Fischinger Moura de Souza, Ida Vanessa Döederlein Schwartz et al. · American Journal of Medical Genetics Part A · 2012 · 19 citations

Life Sciences, Genetics, Molecular Genetics +15

Are MPS II heterozygotes actually asymptomatic? A study based on clinical and biochemical data, X‐inactivation analysis and imaging evaluations

Louise Lapagesse de Camargo Pinto, Sharbel Weidner Maluf, Sandra Leistner‐Segal et al. · American Journal of Medical Genetics Part A · 2010 · 16 citations

Life Sciences, Genetics, Neurology +14

Detailed analysis of X chromosome inactivation in a 49,XXXXX pentasomy

Lúcia Moraes, Leila C.A. Cardoso, Vera LS Moura et al. · Molecular Cytogenetics · 2009 · 16 citations · Full text

Life Sciences, Genetics, Molecular Genetics +10

A <i>de novo</i> complex chromosomal rearrangement with nine breakpoints characterised by FISH in a boy with mild mental retardation, developmental delay, short stature and microcephaly

José Carlos Cabral de Almeida, Antonio Abílio Santa Rose, Patrícia Correia et al. · Clinical Genetics · 1999 · 11 citations

Life Sciences, Genetics, Molecular Genetics +17