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Publications by F.I.V. Errera

Variable Expressivity of Osteogenesis Imperfecta in a Brazilian Family Due to p.G1079S Mutation in the COL1A1 Gene

Genetics and Molecular Research

English

Association of Polymorphisms at the ADIPOR1 Regulatory Region With Type 2 Diabetes and Body Mass Index in a Brazilian Population With European or African Ancestry

Brazilian Journal of Medical and Biological Research

English

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A Novel COL1A1 Gene-Splicing Mutation (C.1875+1G>C) in a Brazilian Patient With Osteogenesis Imperfecta

Genetics and Molecular Research

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Splice Receptor-Site Mutation C.697-2a>g of the COL1A1 Gene in a Chinese Family With Osteogenesis Imperfecta

Intractable and Rare Diseases Research

Medicine

2019

English

Structural Models of Osteogenesis Imperfecta-Associated Variants in the COL1A1 Gene

Molecular and Cellular Proteomics

English

A Novel De Novo COL1A1 Mutation in a Thai Boy With Osteogenesis Imperfecta Born to Consanguineous Parents

Genetics and Molecular Biology

Genetics

Molecular Biology

2017

English

Heterozygous Mutation of C.3521C>T in COL1A1 May Cause Mild Osteogenesis Imperfecta/Ehlers-Danlos Syndrome in a Chinese Family

Intractable and Rare Diseases Research

Medicine

2015

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Correction To: Novel Mutation G324C in WNT1 Mapped in a Large Pakistani Family With Severe Recessively Inherited Osteogenesis Imperfecta

Journal of Biomedical Science

Clinical Biochemistry

English

Alternative Splicing Caused by a Large Deletion in Col1a1 Gene Is Responsible for a Severe Case of Osteogenesis Imperfecta Type Iii. † 853

English

Frameshift Mutation Near the 3' End of the COL1A1 Gene of Type I Collagen Predicts an Elongated Pro Alpha 1(I) Chain and Results in Osteogenesis Imperfecta Type I.

Journal of Clinical Investigation

Medicine

1990

English

Osteogenesis Imperfecta

2004

English

Amanote Research

Discover open access scientific publications

Search, annotate, share and cite publications

Publications by F.I.V. Errera

Variable Expressivity of Osteogenesis Imperfecta in a Brazilian Family Due to p.G1079S Mutation in the COL1A1 Gene

Association of Polymorphisms at the ADIPOR1 Regulatory Region With Type 2 Diabetes and Body Mass Index in a Brazilian Population With European or African Ancestry

Related publications

A Novel COL1A1 Gene-Splicing Mutation (C.1875+1G>C) in a Brazilian Patient With Osteogenesis Imperfecta

Splice Receptor-Site Mutation C.697-2a>g of the COL1A1 Gene in a Chinese Family With Osteogenesis Imperfecta

Structural Models of Osteogenesis Imperfecta-Associated Variants in the COL1A1 Gene

A Novel De Novo COL1A1 Mutation in a Thai Boy With Osteogenesis Imperfecta Born to Consanguineous Parents

Heterozygous Mutation of C.3521C&gt;T in COL1A1 May Cause Mild Osteogenesis Imperfecta/Ehlers-Danlos Syndrome in a Chinese Family

Correction To: Novel Mutation G324C in WNT1 Mapped in a Large Pakistani Family With Severe Recessively Inherited Osteogenesis Imperfecta

Alternative Splicing Caused by a Large Deletion in Col1a1 Gene Is Responsible for a Severe Case of Osteogenesis Imperfecta Type Iii. † 853

Frameshift Mutation Near the 3' End of the COL1A1 Gene of Type I Collagen Predicts an Elongated Pro Alpha 1(I) Chain and Results in Osteogenesis Imperfecta Type I.

Osteogenesis Imperfecta

Heterozygous Mutation of C.3521C>T in COL1A1 May Cause Mild Osteogenesis Imperfecta/Ehlers-Danlos Syndrome in a Chinese Family