B. Theophilus

发表

Novel characterization of a breakpoint in F8: an individualized approach to gene analysis when PCR and MLPA results contradict

J. Oldenburg, O. el-Maarri, M. D. Williams, 2015, Haemophilia : the official journal of the World Federation of Hemophilia.

Independent occurrence of the novel Arg2163 to His mutation in the factor VIII gene in three unrelated families with haemophilia A with different phenotypes

S. Antonarakis, H. Kazazian, F. Hill, 1998 .

Comparison of RNase A, a chemical cleavage and GC-clamped denaturing gradient gel electrophoresis for the detection of mutations in exon 9 of the human acid beta-glucosidase gene.

B. Theophilus, G. Grabowski, F. Smith, 1989, Nucleic acids research.

Internal labeling of DNA probes.

R. Rapley, B. Theophilus, 2002, Methods in molecular biology.

Heterogeneity of mutations in the acid beta-glucosidase gene of Gaucher disease patients.

B. Theophilus, G. Grabowski, F. Smith, 1991, DNA and cell biology.

Gaucher disease: molecular heterogeneity and phenotype-genotype correlations.

B. Theophilus, G. Grabowski, F. Smith, 1989, American journal of human genetics.

Site and type of mutations in the factor VIII gene in patients and carriers of haemophilia A.

F. Hill, B. Theophilus, M. S. Enayat, 2001 .

Preparation and analysis of DNA sequencing gels.

B. Theophilus, 1996, Methods in molecular biology.

Mutation Analysis in F9 Gene of 17 Families with Haemophilia B from Iran

S. Farjadian, M. Karimi, F. Hill, 2004, Haemophilia : the official journal of the World Federation of Hemophilia.

Site and type of mutations in the factor VIII gene in patients and carriers of haemophilia A

M. Williams, F. Hill, M. D. Williams, 2001, Haemophilia : the official journal of the World Federation of Hemophilia.

PCR Mutation Detection Protocols

R. Rapley, B. Theophilus, 2002, Methods in Molecular Biology.

Complex alleles of the acid beta-glucosidase gene in Gaucher disease.

B. Theophilus, G. Grabowski, F. Smith, 1990, American journal of human genetics.

Gender and the stigma of onchocercal skin disease in Africa.

Sunday Samson Babalola, M. Weiss, C. Vlassoff, 2000, Social science & medicine.

Confirmation of genetic testing results in haemostasis and thrombosis – survey of current practice in the field

D. Perry, S. Kitchen, A. Goodeve, 2016, Haemophilia : the official journal of the World Federation of Hemophilia.

Analysis of transcription from the trfA promoter of broad host range plasmid RK2 in Escherichia coli, Pseudomonas putida, and Pseudomonas aeruginosa.

Christopher M Thomas, B. Theophilus, W. Tacon, 1987, Plasmid.

A New Candidate Missense Mutation (Leu 1657 Ile) in an Apparently Asymptomatic Type 2A (Phenotype IIA) von Willebrand Disease Family

F. Hill, B. Theophilus, A. Guilliatt, 2000, Thrombosis and Haemostasis.

Principles and Medical Applications of the Polymerase Chain Reaction

B. Theophilus, 2005 .

Deletions and duplications in the factor VIII gene identified using multiplex ligation‐dependent probe amplification

J. Motwani, M. Williams, B. Theophilus, 2011, Journal of thrombosis and haemostasis : JTH.

De novo mutation causing sporadic type 2A von Willebrancd's disease: report of three cases

K. Pasi, F. Hill, B. Theophilus, 1996, Haemophilia.

Demographic Distribution of Oculoplastic Disorders in Port Harcourt Nigeria

B. Theophilus, N. Chinawa, C. Ejimadu, 2019, Ophthalmology Research: An International Journal.

Identification of a seventh operon on plasmid RK2 regulated by the korA gene product.

Christopher M Thomas, L. Johnston, R. Lurz, 1990, Gene.

Regulation of the trfA and trfB promoters of broad host range plasmid RK2: identification of sequences essential for regulation by trfB/korA/korD.

C. Smith, B. Theophilus, M. Cross, 1985, Nucleic acids research.

Nucleotide sequence of the transcriptional repressor gene korB which plays a key role in regulation of the copy number of broad host range plasmid RK2.

Christopher M Thomas, B. Theophilus, 1987, Nucleic Acids Research.

Genomic DNA Libraries

B. Theophilus, 1998 .