Maria de Fátima de Faria Soares

Novel Deletion of <b><i>SERPINF1</i></b> Causes Autosomal Recessive Osteogenesis Imperfecta Type VI in Two Brazilian Families

Renata Moldenhauer Minillo, Nara Sobreira, Maria de Fátima de Faria Soares et al. · Molecular Syndromology · 2014 · 22 citations · Full text

Novel Deletion, Oi Type Vi, Genetics +18

Abdominal radiograph in the assessment of fecal impaction in children with functional constipation: comparing three scoring systems

Tatyana Borges da Cunha, Soraia Tahan, Maria de Fátima de Faria Soares et al. · Jornal de Pediatria · 2012 · 19 citations · Full text

Overlapping phenotype comprising <scp>Kenny‐Caffey</scp> type 2 and <scp>Sanjad‐Sakati</scp> syndromes: The first case report

Thiago R. Cavole, Eduardo Perrone, Maria de Fátima de Faria Soares et al. · American Journal of Medical Genetics Part A · 2020 · 14 citations

Gomez–López–Hernández syndrome: A case report with clinical and molecular evaluation and literature review

Eduardo Perrone, Vânia D’Almeida, Nara Sobreira et al. · American Journal of Medical Genetics Part A · 2020 · 13 citations · Full text

Developmental Anomaly, Gomez-lópez-hernández Syndrome, Mendelian Disorder +12

Untreated Congenital Hypothyroidism Mimicking Hirschsprung Disease: A Puzzling Case in a One‐Year‐Old Child

Soraia Tahan, Adriana Aparecida Siviero‐Miachon, Maria de Fátima de Faria Soares et al. · Case Reports in Pediatrics · 2018 · 10 citations · Full text