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Subtle chromosomal rearrangements in children with unexplained mental retardation

The Lancet (British edition), 1999-11, Vol.354 (9191), p.1676-1681

1999

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A Comprehensive Screen for TWIST Mutations in Patients with Craniosynostosis Identifies a New Microdeletion Syndrome of Chromosome Band 7p21.1

American journal of human genetics, 1998-11, Vol.63 (5), p.1282-1293

1998

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Del(18p) shown to be a cryptic translocation using a multiprobe FISH assay for subtelomeric chromosome rearrangements

Journal of medical genetics, 1998-09, Vol.35 (9), p.722-726

1998

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Rupture of the ascending aorta caused by blunt trauma

The Annals of thoracic surgery, 1998-07, Vol.66 (1), p.113-117

1998

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Chromosomal Stabilisation by a Subtelomeric Rearrangement Involving Two Closely Related Alu Elements

Human molecular genetics, 1996-08, Vol.5 (8), p.1163-1169

1996

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A mitotically stable marker chromosome negative for whole chromosome libraries, centromere probes and chromosome specific telomere regions: a novel class of supernumerary marker chromosome?

Cytogenetic and genome research, 2001-01, Vol.92 (1-2), p.69-73

2001

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Unilateral Giant Bullous Emphysema With Placental Transmogrification of the Lung

The Annals of thoracic surgery, 1997-07, Vol.64 (1), p.226-228

1997

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Management of the uncontrollable pulmonary air leak with cyanoacrylate glue

The Annals of thoracic surgery, 1997-05, Vol.63 (5), p.1492-1493

1997

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Sequence, structure and pathology of the fully annotated terminal 2 Mb of the short arm of human chromosome 16

Human molecular genetics, 2001-02, Vol.10 (4), p.339-352

2001

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Refinement of the Alpha Aminooleic Acid Bioprosthetic Valve Anticalcification Technique

The Annals of thoracic surgery, 1997-07, Vol.64 (1), p.50-58

1997

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Development and Clinical Application of an Innovative Fluorescence in situ Hybridization Technique Which Detects Submicroscopic Rearrangements Involving Telomeres

European journal of human genetics : EJHG, 1997-01, Vol.5 (1), p.1-8

1997

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Monosomy for the most telomeric, gene-rich region of the short arm of human chromosome 16 causes minimal phenotypic effects

European journal of human genetics : EJHG, 2001-03, Vol.9 (3), p.217-225

2001

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Identification of a subtle t(16;19)(p13.3;p13.3) in an infant with multiple congenital abnormalities using a 12-colour multiplex FISH telomere assay, M-TEL

European journal of human genetics : EJHG, 2000-12, Vol.8 (12), p.903-910

2000

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Translocation between chromosome 5q35 and chromosome 11q13 - an unusual cytogenetic finding in a primary refractory acute myeloid leukemia

Clinical and laboratory haematology, 2006-06, Vol.28 (3), p.160-163

2006

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Warm blood cardioplegia: Superior protection after acute myocardial ischemia

The Annals of thoracic surgery, 1993, Vol.55 (1), p.32-42

1993

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Incompletely penetrant PKD1 alleles suggest a role for gene dosage in cyst initiation in polycystic kidney disease

Kidney international, 2010-02, Vol.77 (4), p.368

2010

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Subtelomeric familial translocation t(2;7)(q37;q35) leading to partial trisomy 7q35→qter: Molecular cytogenetic analysis and clinical phenotype in two generations

American journal of medical genetics, 2000-08, Vol.93 (5), p.349-354

2000

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Characterisation of X;17(q12;p13) Translocation Breakpoints in a Female Patient with Hypomelanosis of Ito and Choroid Plexus Papilloma

European journal of human genetics : EJHG, 1997-03, Vol.5 (2), p.61-68

1997

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Molecular cytogenetics in haematological malignancy: current technology and future prospects

Chromosoma, 2005-09, Vol.114 (4), p.286-294

2005

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Incompletely penetrant PKD1 alleles suggest a role for gene dosage in cyst initiation in polycystic kidney disease

Kidney international, 2009-06, Vol.75 (12), p.1359

2009

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Ground Water Resources Assessment for the Municipality of Shenyang, China

Ground water monitoring & remediation, 1994, Vol.14 (2), p.92-94

Horsley, Scott W.

1994

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Revascularization for acute regional infarct: Superior protection with warm blood cardioplegia

The Annals of thoracic surgery, 1993-12, Vol.56 (6), p.1228-1238

1993

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Myocardial protection for coronary artery bypass in patients with acute myocardial infarction: resuscitation of ischemic myocardium

Seminars in thoracic and cardiovascular surgery, 1995-10, Vol.7 (4), p.191-197

1995

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Rapid mapping of markers applying vectorette technology to YAC fragmentation allows easy assembly of a high-density STS bacterial clone contig spanning the markers D6S1260-D6S1918

Mammalian genome, 1998-03, Vol.9 (3), p.220-225

1998

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Array CGH of fusion gene-positive leukemia-derived cell lines reveals cryptic regions of genomic gain and loss

Genes chromosomes & cancer, 2006-06, Vol.45 (6), p.554-564

2006

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Subtle chromosomal rearrangements in children with unexplained mental retardation

A Comprehensive Screen for TWIST Mutations in Patients with Craniosynostosis Identifies a New Microdeletion Syndrome of Chromosome Band 7p21.1

Del(18p) shown to be a cryptic translocation using a multiprobe FISH assay for subtelomeric chromosome rearrangements

Rupture of the ascending aorta caused by blunt trauma

Chromosomal Stabilisation by a Subtelomeric Rearrangement Involving Two Closely Related Alu Elements

A mitotically stable marker chromosome negative for whole chromosome libraries, centromere probes and chromosome specific telomere regions: a novel class of supernumerary marker chromosome?

Unilateral Giant Bullous Emphysema With Placental Transmogrification of the Lung

Management of the uncontrollable pulmonary air leak with cyanoacrylate glue

Sequence, structure and pathology of the fully annotated terminal 2 Mb of the short arm of human chromosome 16

Refinement of the Alpha Aminooleic Acid Bioprosthetic Valve Anticalcification Technique

Development and Clinical Application of an Innovative Fluorescence in situ Hybridization Technique Which Detects Submicroscopic Rearrangements Involving Telomeres

Monosomy for the most telomeric, gene-rich region of the short arm of human chromosome 16 causes minimal phenotypic effects

Identification of a subtle t(16;19)(p13.3;p13.3) in an infant with multiple congenital abnormalities using a 12-colour multiplex FISH telomere assay, M-TEL

Translocation between chromosome 5q35 and chromosome 11q13 - an unusual cytogenetic finding in a primary refractory acute myeloid leukemia

Warm blood cardioplegia: Superior protection after acute myocardial ischemia

Incompletely penetrant PKD1 alleles suggest a role for gene dosage in cyst initiation in polycystic kidney disease

Subtelomeric familial translocation t(2;7)(q37;q35) leading to partial trisomy 7q35→qter: Molecular cytogenetic analysis and clinical phenotype in two generations

Characterisation of X;17(q12;p13) Translocation Breakpoints in a Female Patient with Hypomelanosis of Ito and Choroid Plexus Papilloma

Molecular cytogenetics in haematological malignancy: current technology and future prospects

Incompletely penetrant PKD1 alleles suggest a role for gene dosage in cyst initiation in polycystic kidney disease

Ground Water Resources Assessment for the Municipality of Shenyang, China

Revascularization for acute regional infarct: Superior protection with warm blood cardioplegia

Myocardial protection for coronary artery bypass in patients with acute myocardial infarction: resuscitation of ischemic myocardium

Rapid mapping of markers applying vectorette technology to YAC fragmentation allows easy assembly of a high-density STS bacterial clone contig spanning the markers D6S1260-D6S1918

Array CGH of fusion gene-positive leukemia-derived cell lines reveals cryptic regions of genomic gain and loss

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