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Localization of a gene for autosomal dominant nocturnal frontal lobe epilepsy to chromosome 20q13.2

Nature genetics, 1995-05, Vol.10 (1), p.117-118

1995

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Autosomal Dominant Nocturnal Frontal-Lobe Epilepsy: Genetic Heterogeneity and Evidence for a Second Locus at 15q24

American journal of human genetics, 1998-10, Vol.63 (4), p.1108-1116

1998

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Capecitabine combined with oxaliplatin (CapOx) in clinical practice: how significant is peripheral neuropathy?

Annals of oncology, 2010-08, Vol.21 (8), p.1657-1661

2010

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Biosorption of heavy metals by Saccharomyces cerevisiae

Applied microbiology and biotechnology, 1995, Vol.42 (5), p.797-806

1995

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Incidence and origin of null alleles in the (AC)n microsatellite markers

American journal of human genetics, 1993-05, Vol.52 (5), p.922-927

1993

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Reply to capecitabine combined with oxaliplatin (CapOx) in clinical practice: how significant is peripheral neuropathy?

Annals of oncology, 2011-01, Vol.22 (1), p.240-241

2011

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Short Course Preoperative Radiotherapy for Rectal Cancer

Clinical oncology (Royal College of Radiologists (Great Britain)), 2006-10, Vol.18 (8), p.591-593

Phillips, H.A.

2006

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Media for hybridoma growth and monoclonal antibody production

Biotechnology Advances, 1988, Vol.6 (2), p.169-182

1988

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Bladder carcinoma in the elderly: Is there a role for split radical radiotherapy?

Clinical oncology (Royal College of Radiologists (Great Britain)), 1996, Vol.8 (2), p.129-130

1996

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The Role of the p53 Tumour Suppressor Gene in Human Breast Cancer

Clinical Oncology, 1999-01, Vol.11 (3), p.148-155

Phillips, H.A.

1999

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1268 Laser palliation for colorectal tumours: evaluating effectiveness and quality of life

European journal of cancer supplements, 2003-09, Vol.1 (5), p.S384-S384

2003

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On the direct determination of metals in lubricating oils by ICP

Spectrochimica acta. Part B: Atomic spectroscopy, 1985, Vol.40 (10), p.1447-1456

1985

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A pilot study of the use of p53 gene mutations as a biochemical marker for bladder cancer in bladder washing samples

Clinical oncology (Royal College of Radiologists (Great Britain)), 1997, Vol.9 (2), p.131-131

1997

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Nipple aspirate fluid in relation to breast cancer

Breast (Edinburgh), 1999-08, Vol.8 (4), p.169-174

1999

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A cysteine endopeptidase from barley malt which degrades hordein

Phytochemistry (Oxford), 1989, Vol.28 (12), p.3285-3290

1989

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Testicular Seminoma in a Patient with Ataxia-Telangiectasia

Clinical oncology (Royal College of Radiologists (Great Britain)), 1999-01, Vol.11 (1), p.63-64

1999

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A PCR-Based Genetic Linkage Map of Human Chromosome 16

Genomics (San Diego, Calif.), 1994-07, Vol.22 (1), p.68-76

1994

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Refined genetic localization for central core disease

American journal of human genetics, 1993-02, Vol.52 (2), p.398-405

1993

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Isolation and Characterization of Transcribed Sequences from a Chromosome 16 hn-cDNA Library and the Physical Mapping of Genes and Transcribed Sequences Using a High-Resolution Somatic Cell Panel of Human Chromosome 16

Genomics (San Diego, Calif.), 1994-03, Vol.20 (2), p.169-175

1994

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Split course radical radiotherapy for bladder cancer in the elderly: Nonsense or commonsense? A report of 76 patients

Clinical oncology (Royal College of Radiologists (Great Britain)), 1996, Vol.8 (1), p.35-38

1996

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Absence of mutations in sites of key functional importance of the RIα and RIIβ regulatory subunits of protein kinase A in human breast cancers

Breast (Edinburgh), 1998-06, Vol.7 (3), p.139-142

1998

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Dinculeotide repear polymorphisms at the D16S164, D16S168 and D16S186 loci at 1621-q22.1

Nucleic acids research, 1991-12, Vol.19 (24), p.6964-6964

1991

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Overcoming Separation Anxiety

Process Cooling & Equipment (Online), 2008-05

2008

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Localization of the human gene for [mu]-crystallin to chromosome 16p

Genomics (San Diego, Calif.), 1992-12, Vol.14:4

1992

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Genetic linkage studies in familial frontal epilepsy: Exclusion of the human chromosome regions homologous to the El-1 mouse locus

Epilepsy research, 1995-11, Vol.22 (3), p.227-233

1995

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Localization of a gene for autosomal dominant nocturnal frontal lobe epilepsy to chromosome 20q13.2

Autosomal Dominant Nocturnal Frontal-Lobe Epilepsy: Genetic Heterogeneity and Evidence for a Second Locus at 15q24

Capecitabine combined with oxaliplatin (CapOx) in clinical practice: how significant is peripheral neuropathy?

Biosorption of heavy metals by Saccharomyces cerevisiae

Incidence and origin of null alleles in the (AC)n microsatellite markers

Reply to capecitabine combined with oxaliplatin (CapOx) in clinical practice: how significant is peripheral neuropathy?

Short Course Preoperative Radiotherapy for Rectal Cancer

Media for hybridoma growth and monoclonal antibody production

Bladder carcinoma in the elderly: Is there a role for split radical radiotherapy?

The Role of the p53 Tumour Suppressor Gene in Human Breast Cancer

1268 Laser palliation for colorectal tumours: evaluating effectiveness and quality of life

On the direct determination of metals in lubricating oils by ICP

A pilot study of the use of p53 gene mutations as a biochemical marker for bladder cancer in bladder washing samples

Nipple aspirate fluid in relation to breast cancer

A cysteine endopeptidase from barley malt which degrades hordein

Testicular Seminoma in a Patient with Ataxia-Telangiectasia

A PCR-Based Genetic Linkage Map of Human Chromosome 16

Refined genetic localization for central core disease

Isolation and Characterization of Transcribed Sequences from a Chromosome 16 hn-cDNA Library and the Physical Mapping of Genes and Transcribed Sequences Using a High-Resolution Somatic Cell Panel of Human Chromosome 16

Split course radical radiotherapy for bladder cancer in the elderly: Nonsense or commonsense? A report of 76 patients

Absence of mutations in sites of key functional importance of the RIα and RIIβ regulatory subunits of protein kinase A in human breast cancers

Dinculeotide repear polymorphisms at the D16S164, D16S168 and D16S186 loci at 1621-q22.1

Overcoming Separation Anxiety

Localization of the human gene for [mu]-crystallin to chromosome 16p

Genetic linkage studies in familial frontal epilepsy: Exclusion of the human chromosome regions homologous to the El-1 mouse locus

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