Concepedia

Milene Mulatinho

MM

Statistics

Publications

5

Citations

198

H-Index

5

Active since

2008

Affiliations

Fundação Oswaldo Cruz(Current)

University of California, Los Angeles

Universidade Federal do Rio de Janeiro

Jena University Hospital

Milene Mulatinho is an author at Fundação Oswaldo Cruz specializing in genetics, molecular genetics, and life sciences.

Publications per year

2008–2017

5

Publications

5

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

, , +11

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 · 54 citations · Full text

, , +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

, , +17

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

, , +17

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

, , +16

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