Milene Mulatinho

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

De novo loss‐of‐function variants in <i>STAG2</i> are associated with developmental delay, microcephaly, and congenital anomalies

Sureni V. Mullegama, Steven D. Klein, Milene Mulatinho et al. · American Journal of Medical Genetics Part A · 2017 · 53 citations · Full text

Genetics, Congenital Anomalies, Molecular Genetics +17

Severe intellectual disability, omphalocele, hypospadia and high blood pressure associated to a deletion at 2q22.1q22.3: case report

Milene Mulatinho, Cassio Luiz de Carvalho Serao, Fernanda B. Scalco et al. · Molecular Cytogenetics · 2012 · 40 citations · Full text

A New Multicolor Fluorescence In Situ Hybridization Probe Set Directed Against Human Heterochromatin

Maria Bucksch, Monika Ziegler, Nadezda Kosayakova et al. · Journal of Histochemistry & Cytochemistry · 2012 · 19 citations · Full text

Cytogenetics, Genetics, Molecular Biology +18

Deletion (1)(p32.2–p32.3) detected by array‐CGH in a patient with developmental delay/mental retardation, dysmorphic features and low cholesterol: A new microdeletion syndrome?

Milene Mulatinho, Juan Clinton Llerena, Trond P. Leren et al. · American Journal of Medical Genetics Part A · 2008 · 12 citations

Genetics, Molecular Genetics, Disease Gene Identification +19