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Cloning defined regions of the human genome by microdissection of banded chromosomes and enzymatic amplification

Nature (London), 1989-03, Vol.338 (6213), p.348-350

1989

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Physical map of human 6p21.2-6p21.3: region flanking the centromeric end of the major histocompatibility complex

Genome research, 1998-06, Vol.8 (6), p.631-643

1998

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Microdissection of banded human chromosomes

Human genetics, 1990-05, Vol.84 (6), p.507-511

1990

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Homologous sequences at human chromosome 9 bands p12 and q13-21.1 are involved in different patterns of pericentric rearrangements

European journal of human genetics : EJHG, 2002-12, Vol.10 (12), p.790-800

2002

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Construction and characterization of band-specific DNA libraries

Human genetics, 1990-05, Vol.84 (6), p.512-516

1990

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Overrepresentation of small supernumerary marker chromosomes (sSMC) from chromosome 6 origin in cases with multiple sSMC

American journal of medical genetics. Part A, 2006-01, Vol.140A (1), p.46-51

2006

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Two new cases of analphoid marker chromosomes

American journal of medical genetics, 2003-01, Vol.116A (3), p.284-289

2003

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Cloning of TRAP, a ligand for CD40 on human T cells

European journal of immunology, 1992-12, Vol.22 (12), p.3191-3194

1992

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Proteasome components with reciprocal expression to that of the MHC-encoded LMP proteins

Current biology, 1994-09, Vol.4 (9), p.769-776

1994

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NOT, a human immediate-early response gene closely related to the steroid/thyroid hormone receptor NAK1/TR3

Molecular endocrinology (Baltimore, Md.), 1994-11, Vol.8 (11), p.1583-1591

1994

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Defective Expression of CD40 Ligand on T Cells Causes "X-Linked Immunodeficiency with Hyper-IgM (HIGM1)"

Immunological reviews, 1994-04, Vol.138 (1), p.39-59

1994

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Improved definition of chromosomal breakpoints using high-resolution multicolour banding

Human genetics, 2001-06, Vol.108 (6), p.478-483

2001

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Interstitial deletion of chromosome 6q : precise definition of the breakpoints by microdissection, DNA amplification, and reverse painting

Human genetics, 1996-06, Vol.97 (6), p.705-709

1996

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Maternal insertion of 18q11.2-q12.2 in 18p11.3 of the same chromosome analysed by microdissection and multicolour banding (MCB)

Prenatal diagnosis, 2001-12, Vol.21 (12), p.1049-1052

2001

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Cloning of ATAC, an activation‐induced, chemokine‐related molecule exclusively expressed in CD8+ T lymphocytes

European journal of immunology, 1995-06, Vol.25 (6), p.1744-1748

1995

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A multiple translocation event in a patient with hexadactyly, facial dysmorphism, mental retardation and behaviour disorder characterised comprehensively by molecular cytogenetics. Case report and review of the literature

European journal of pediatrics, 2003-09, Vol.162 (9), p.582-588

2003

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Genomic organization of the human folate receptor genes on chromosome 11q13

Genomics (San Diego, Calif.), 1992-10, Vol.14 (2), p.423-430

1992

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Released chromatin: linearized DNA for high resolution fluorescence in situ hybridization

Human molecular genetics, 1994-08, Vol.3 (8), p.1275-1280

1994

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An easy and reliable procedure of microdissection technique for the analysis of chromosomal breakpoints and marker chromosomes

Chromosome research, 1999-01, Vol.7 (5), p.355-362

1999

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A testis-expressed Zn finger gene (ZNF76) in human 6p21.3 centromeric to the MHC is closely linked to the human homolog of the t-complex gene tcp-11

Genomics (San Diego, Calif.), 1992-11, Vol.14 (3), p.673-679

1992

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Improved detection of chromosome 16 rearrangements in acute myeloid leukemias using 16p and 16q specific microdissection DNA libraries

Oncology reports, 1996-09

1996

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Molecular cytogenetic characterization of del(7q) in two uterine leiomyoma-derived cell lines

Genes chromosomes & cancer, 1997-03, Vol.18 (3), p.155-161

1997

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Nephropathic cystinosis (CTNS-LSB): construction of a YAC contig comprising the refined critical region on chromosome 17p13

European journal of human genetics : EJHG, 1997-01, Vol.5 (1), p.9-14

1997

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Complex chromosomal rearrangements associated with congenital erythrophagocytotic histiocytosis

Clinical genetics, 1998-04, Vol.53 (4), p.298-302

1998

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Microdissection of the Prader-Willi syndrome chromosome region and identification of potential gene sequences

Genomics (San Diego, Calif.), 1990-03, Vol.6 (3), p.521-527

1990

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Cloning defined regions of the human genome by microdissection of banded chromosomes and enzymatic amplification

Physical map of human 6p21.2-6p21.3: region flanking the centromeric end of the major histocompatibility complex

Microdissection of banded human chromosomes

Homologous sequences at human chromosome 9 bands p12 and q13-21.1 are involved in different patterns of pericentric rearrangements

Construction and characterization of band-specific DNA libraries

Overrepresentation of small supernumerary marker chromosomes (sSMC) from chromosome 6 origin in cases with multiple sSMC

Two new cases of analphoid marker chromosomes

Cloning of TRAP, a ligand for CD40 on human T cells

Proteasome components with reciprocal expression to that of the MHC-encoded LMP proteins

NOT, a human immediate-early response gene closely related to the steroid/thyroid hormone receptor NAK1/TR3

Defective Expression of CD40 Ligand on T Cells Causes "X-Linked Immunodeficiency with Hyper-IgM (HIGM1)"

Improved definition of chromosomal breakpoints using high-resolution multicolour banding

Interstitial deletion of chromosome 6q : precise definition of the breakpoints by microdissection, DNA amplification, and reverse painting

Maternal insertion of 18q11.2-q12.2 in 18p11.3 of the same chromosome analysed by microdissection and multicolour banding (MCB)

Cloning of ATAC, an activation‐induced, chemokine‐related molecule exclusively expressed in CD8+ T lymphocytes

A multiple translocation event in a patient with hexadactyly, facial dysmorphism, mental retardation and behaviour disorder characterised comprehensively by molecular cytogenetics. Case report and review of the literature

Genomic organization of the human folate receptor genes on chromosome 11q13

Released chromatin: linearized DNA for high resolution fluorescence in situ hybridization

An easy and reliable procedure of microdissection technique for the analysis of chromosomal breakpoints and marker chromosomes

A testis-expressed Zn finger gene (ZNF76) in human 6p21.3 centromeric to the MHC is closely linked to the human homolog of the t-complex gene tcp-11

Improved detection of chromosome 16 rearrangements in acute myeloid leukemias using 16p and 16q specific microdissection DNA libraries

Molecular cytogenetic characterization of del(7q) in two uterine leiomyoma-derived cell lines

Nephropathic cystinosis (CTNS-LSB): construction of a YAC contig comprising the refined critical region on chromosome 17p13

Complex chromosomal rearrangements associated with congenital erythrophagocytotic histiocytosis

Microdissection of the Prader-Willi syndrome chromosome region and identification of potential gene sequences

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