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Chromosome analysis of blastomeres from human embryos by using comparative genomic hybridization

Human genetics, 2000-02, Vol.106 (2), p.210-217

2000

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Chromosome abnormalities identified by comparative genomic hybridization in embryos from women with repeated implantation failure

Molecular human reproduction, 2002-11, Vol.8 (11), p.1035-1041

2002

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Site-specific, Rep-mediated integration of the intact β-globin locus in the human erythroleukaemic cell line K562

Gene therapy, 2008-10, Vol.15 (20), p.1372-1383

2008

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The transient expression of mRNA coding for Rep protein from AAV facilitates targeted plasmid integration

The journal of gene medicine, 2008-01, Vol.10 (1), p.42-50

2008

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A functional marker centromere with no detectable alpha-satellite, satellite III, or CENP-B protein : activation of a latent centromere ?

American journal of human genetics, 1993-06, Vol.52 (6), p.1153-1163

1993

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Association of a chromosome deletion syndrome with a fragile site within the proto-oncogene CBL2

Nature (London), 1995-07, Vol.376 (6536), p.145-149

1995

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Preimplantation aneuploidy screening using comparative genomic hybridization or fluorescence in situ hybridization of embryos from patients with recurrent implantation failure

Fertility and sterility, 2003-10, Vol.80 (4), p.860-868

2003

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Fetal nucleated red blood cells from CVS washings: an aid to development of first trimester non-invasive prenatal diagnosis

Prenatal diagnosis, 2001-10, Vol.21 (10), p.827-834

2001

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Olfactory Receptor–Gene Clusters, Genomic-Inversion Polymorphisms, and Common Chromosome Rearrangements

American journal of human genetics, 2001-04, Vol.68 (4), p.874-883

2001

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Distal 8p deletion (8p23.1----8pter): a common deletion?

Journal of medical genetics, 1992-06, Vol.29 (6), p.407-411

1992

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Asymmetry and skin pigmentary anomalies in chromosome mosaicism

Journal of medical genetics, 1994-09, Vol.31 (9), p.694-701

1994

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Directly inherited partial trisomy of chromosome 6p identified in a father and daughter by chromosome microdissection

Journal of medical genetics, 1999-04, Vol.36 (4), p.335-338

1999

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Comparative chromosome painting between marsupial orders: relationships with a 2n = 14 ancestral marsupial karyotype

Chromosome research, 1999-01, Vol.7 (7), p.509-517

1999

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A humanized BAC transgenic/knockout mouse model for HbE/β-thalassemia

Genomics (San Diego, Calif.), 2006-09, Vol.88 (3), p.309-315

2006

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Humanized β-Thalassemia Mouse Model Containing the Common IVSI-110 Splicing Mutation

The Journal of biological chemistry, 2006-03, Vol.281 (11), p.7399-7405

2006

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Chromosomal painting detects non-random chromosome arrangement in dasyurid marsupial sperm

Chromosome research, 2001-04, Vol.9 (3), p.251-259

2001

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Chromosomal duplication of band 10p14 segregating through four generations

Journal of medical genetics, 2000-03, Vol.37 (3), p.233-237

2000

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Evidence that Rieger syndrome maps to 4q25 or 4q27

Journal of medical genetics, 1992-04, Vol.29 (4), p.256-258

1992

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Site-specific, Rep-mediated integration of the intact [beta]-globin locus in the human erythroleukaemic cell line K562

Gene therapy, 2008-11, Vol.15 (20), p.1372-1383

2008

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Chromatin-binding regions of EBNA1 protein facilitate the enhanced transfection of Epstein-Barr virus-based vectors

Human gene therapy, 2006-08, Vol.17 (8), p.833-844

2006

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Transient expression of AAV rep protein facilitates targeted integration of a 200 kb BAC containing the entire beta-globin locus

Blood cells, molecules, & diseases, 2008-03, Vol.40 (2), p.288-288

2008

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Five cases demonstrating the distinctive behavioural features of chromosome deletion 17(p 11.2 p 11.2) (Smith-Magenis syndrome)

Journal of paediatrics and child health, 1990-02, Vol.26 (1), p.17-21

1990

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Deletion of a 5-cM region at chromosome 8p23 is associated with a spectrum of congenital heart defects

Circulation (New York, N.Y.), 2000-07, Vol.102 (4), p.432-437

2000

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Human BAC-mediated rescue of the Friedreich ataxia knockout mutation in transgenic mice

Mammalian genome, 2004-05, Vol.15 (5), p.370-382

2004

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Minute Y chromosome derived marker in a child with gonadoblastoma: cytogenetic and DNA studies

Journal of medical genetics, 1992-08, Vol.29 (8), p.542-546

1992

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Chromosome analysis of blastomeres from human embryos by using comparative genomic hybridization

Chromosome abnormalities identified by comparative genomic hybridization in embryos from women with repeated implantation failure

Site-specific, Rep-mediated integration of the intact β-globin locus in the human erythroleukaemic cell line K562

The transient expression of mRNA coding for Rep protein from AAV facilitates targeted plasmid integration

A functional marker centromere with no detectable alpha-satellite, satellite III, or CENP-B protein : activation of a latent centromere ?

Association of a chromosome deletion syndrome with a fragile site within the proto-oncogene CBL2

Preimplantation aneuploidy screening using comparative genomic hybridization or fluorescence in situ hybridization of embryos from patients with recurrent implantation failure

Fetal nucleated red blood cells from CVS washings: an aid to development of first trimester non-invasive prenatal diagnosis

Olfactory Receptor–Gene Clusters, Genomic-Inversion Polymorphisms, and Common Chromosome Rearrangements

Distal 8p deletion (8p23.1----8pter): a common deletion?

Asymmetry and skin pigmentary anomalies in chromosome mosaicism

Directly inherited partial trisomy of chromosome 6p identified in a father and daughter by chromosome microdissection

Comparative chromosome painting between marsupial orders: relationships with a 2n = 14 ancestral marsupial karyotype

A humanized BAC transgenic/knockout mouse model for HbE/β-thalassemia

Humanized β-Thalassemia Mouse Model Containing the Common IVSI-110 Splicing Mutation

Chromosomal painting detects non-random chromosome arrangement in dasyurid marsupial sperm

Chromosomal duplication of band 10p14 segregating through four generations

Evidence that Rieger syndrome maps to 4q25 or 4q27

Site-specific, Rep-mediated integration of the intact [beta]-globin locus in the human erythroleukaemic cell line K562

Chromatin-binding regions of EBNA1 protein facilitate the enhanced transfection of Epstein-Barr virus-based vectors

Transient expression of AAV rep protein facilitates targeted integration of a 200 kb BAC containing the entire beta-globin locus

Five cases demonstrating the distinctive behavioural features of chromosome deletion 17(p 11.2 p 11.2) (Smith-Magenis syndrome)

Deletion of a 5-cM region at chromosome 8p23 is associated with a spectrum of congenital heart defects

Human BAC-mediated rescue of the Friedreich ataxia knockout mutation in transgenic mice

Minute Y chromosome derived marker in a child with gonadoblastoma: cytogenetic and DNA studies

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