P. Matthews

发表

Multiple genetic diagnoses from single cells using multiplex PCR: reliability and allele dropout

P. Quirke, I. Findlay, P. Matthews, 1998, Prenatal diagnosis.

Identifying the Origin of Single Corneal Cells by DNA Fingerprinting: Part II – Application to Limbal Allografting

I. Findlay, B. Noble, P. Matthews, 2001, Cornea.

Identifying the Origin of Single Corneal Cells by DNA Fingerprinting: Part I – Implications for Corneal Limbal Allografting

I. Findlay, B. Noble, P. Matthews, 2001, Cornea.

Preimplantation Genetic Diagnosis Using Fluorescent Polymerase Chain Reaction: Results and Future Developments

P. Quirke, I. Findlay, P. Matthews, 1999, Journal of Assisted Reproduction and Genetics.

Using MF-PCR to diagnose multiple defects from single cells: implications for PGD

K. Mitchelson, I. Findlay, P. Matthews, 2001, Molecular and Cellular Endocrinology.

Rapid Trisomy Diagnosis (21, 18, and 13) Using Fluorescent PCR and Short Tandem Repeats: Applications for Prenatal Diagnosis and Preimplantation Genetic Diagnosis

P. Quirke, T. Marton, Z. Papp, 1998, Journal of Assisted Reproduction and Genetics.

Same day diagnosis of Down's syndrome and sex in single cells using multiplex fluorescent PCR.

P. Quirke, Z. Papp, T. Tóth, 1998, Molecular pathology : MP.

Prenatal diagnosis of tetrasomy 18p using multiplex fluorescent PCR and comparison with a variety of techniques.

M. Peters, S. Healey, I. Findlay, 2003, Genetic testing.

Rapid determination of trisomy 18 parental origin using fluorescent PCR and small tandem repeat markers: case reports

P. Quirke, T. Marton, Z. Papp, 1998, Clinical Genetics.