Lucilene Ribeiro-Bicudo
Universidade Federal de Goiás - Câmpus Samambaia
15 papers found
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Congenital chromoanagenesis in the routine postnatal chromosomal microarray analyses
UploadCongenital Heart Disease Revealing Familial 22q11 Deletion Syndrome
Download from doi.orgClinical findings in patients with GLI2 mutations – phenotypic variability
Download from www.ncbi.nlm.nih.govSonic hedgehog (SHH) mutation in patients within the spectrum of holoprosencephaly
UploadVariable phenotypic manifestations of a K44N mutation in the TGIF gene
UploadSIX3 mutations with holoprosencephaly
UploadHoloprosencephaly: Clinical evaluation on audiological and brainstem electrophysiological profiles
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