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Survival outcome differences based on treatments used and knowledge of the primary tumour site for patients with cancer of unknown and known primary in Ontario

Current oncology (Toronto), 2018-10, Vol.25 (5), p.307-316

2018

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The clinical significance of occult gynecologic primary tumours in metastatic cancer

Current oncology (Toronto), 2017-10, Vol.24 (5), p.e368-378

2017

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Imprinting-Mutation Mechanisms in Prader-Willi Syndrome

American journal of human genetics, 1999-02, Vol.64 (2), p.397-413

1999

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Relating Centromeric Topography in Fixed Human Chromosomes to α-Satellite DNA and CENP-B Distribution

Cytogenetic and genome research, 2013-01, Vol.139 (4), p.234-242

2013

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Characterization of an African American (AA) subject carrying two novel functional CYP2D6 alleles

Clinical pharmacology and therapeutics, 2003-02, Vol.73 (2), p.P12-P12

2003

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Absence of linkage of apparently single gene mediated ADHD with the human syntenic region of the mouse mutant Coloboma

American journal of medical genetics, 1995-12, Vol.60 (6), p.573-579

1995

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Ab initio exon definition using an information theory-based approach

2009 43rd Annual Conference on Information Sciences and Systems, 2009, p.847-852

Rogan, P.K.

2009

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Bloom syndrome and maternal uniparental disomy for chromosome 15

American journal of human genetics, 1994-07, Vol.55 (1), p.74-80

1994

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A common insertion/deletion polymorphism in the Prader—Willi syndrome minimal critical region

Human molecular genetics, 1994-10, Vol.3 (10), p.1912-1912

1994

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Phylogenetic inference based on information theory-based PCR amplification

Journal of phytopathology, 1998-09, Vol.146 (8/9), p.427-430

1998

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A new missense mutation, Arg719Gln, in the β-cardiac heavy chain myosin gene of patients with familial hypertrophic cardiomyopathy

Human molecular genetics, 1994-09, Vol.3 (9), p.1716-1716

1994

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Hydration in purple membrane as a function of relative humidity

Journal of molecular biology, 1981-01, Vol.145 (1), p.281-284

1981

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High resolution detection of chromosome abnormalities with single copy fluorescence in situ hybridization

2004 2nd IEEE International Symposium on Biomedical Imaging: Nano to Macro (IEEE Cat No. 04EX821), 2004, p.73-76 Vol. 1

2004

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Two-dimensional agarose gel electrophoresis of restriction-digested genomic DNA

Methods (San Diego, Calif.), 1991, Vol.3 (2), p.91-97

1991

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Duplication and loss of chromosome 21 in two children with Down syndrome and acute leukemia

American journal of medical genetics, 1995-11, Vol.59 (2), p.174-181

1995

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Multiple imprinted genes associated with Prader-Willi syndrome and location of an imprinting control element

Acta geneticae medicae et gemellologiae, 1996, Vol.45 (1-2), p.87-89

1996

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Survival outcome differences based on treatments used and knowledge of the primary tumour site for patients with cancer of unknown and known primary in Ontario

The clinical significance of occult gynecologic primary tumours in metastatic cancer

Imprinting-Mutation Mechanisms in Prader-Willi Syndrome

Relating Centromeric Topography in Fixed Human Chromosomes to α-Satellite DNA and CENP-B Distribution

Characterization of an African American (AA) subject carrying two novel functional CYP2D6 alleles

Absence of linkage of apparently single gene mediated ADHD with the human syntenic region of the mouse mutant Coloboma

Ab initio exon definition using an information theory-based approach

Bloom syndrome and maternal uniparental disomy for chromosome 15

A common insertion/deletion polymorphism in the Prader—Willi syndrome minimal critical region

Phylogenetic inference based on information theory-based PCR amplification

A new missense mutation, Arg719Gln, in the β-cardiac heavy chain myosin gene of patients with familial hypertrophic cardiomyopathy

Hydration in purple membrane as a function of relative humidity

High resolution detection of chromosome abnormalities with single copy fluorescence in situ hybridization

Two-dimensional agarose gel electrophoresis of restriction-digested genomic DNA

Duplication and loss of chromosome 21 in two children with Down syndrome and acute leukemia

Multiple imprinted genes associated with Prader-Willi syndrome and location of an imprinting control element

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