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Heloísa B. Pena

Universidade Federal de Minas Gerais

13

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166

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1p13.2 deletion displays clinical features overlapping Noonan syndrome, likely related to NRAS gene haploinsufficiency

2016 Genetics and Molecular Biology
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Accurate, Fast and Cost-Effective Diagnostic Test for Monosomy 1p36 Using Real-Time Quantitative PCR

2014 Disease Markers
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Exome sequencing identifies a novel homozygous variant in NDRG4 in a family with infantile myofibromatosis

2014 European Journal of Medical Genetics
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Simple, Rapid and Inexpensive Quantitative Fluorescent PCR Method for Detection of Microdeletion and Microduplication Syndromes

2013 PLOS ONE
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Automated Genotyping of a Highly Informative Panel of 40 Short Insertion-Deletion Polymorphisms Resolved in Polyacrylamide Gels for Forensic Identification and Kinship Analysis

2012 Transfusion Medicine and Hemotherapy
- Heloísa B. Pena
- Sérgio D.J. Pena
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Update of the Gene Discovery Program in Schistosoma mansoni with the Expressed Sequence Tag Approach

1997 Memorias Do Instituto Oswaldo Cruz
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Intracellular promiscuity in Schistosoma mansoni: nuclear transcribed DNA sequences are part of a mitochondrial minisatellite region

1995 Proceedings of the National Academy of Sciences of the United States of America
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DNA polymorphism of schistosomes and their snail hosts

1995 Memorias Do Instituto Oswaldo Cruz
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Citations (14)