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A microfluidics approach for the isolation of nucleated red blood cells (NRBCs) from the peripheral blood of pregnant women

Prenatal diagnosis, 2008-10, Vol.28 (10), p.892-899

2008

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Evidence for a Turner Syndrome Locus or Loci at Xp11.2-p22.1

American journal of human genetics, 1998-12, Vol.63 (6), p.1757-1766

1998

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A Gene Involved in XY Sex Reversal Is Located on Chromosome 9, Distal to Marker D9S1779

American journal of human genetics, 1998-09, Vol.63 (3), p.794-802

1998

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Molecular cytogenetic analysis of Inv Dup(15) chromosomes, using probes specific for the Prader-Willi/Angelman syndrome region : clinical implications

American journal of human genetics, 1994-05, Vol.54 (5), p.748-756

1994

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Correction of Xeroderma Pigmentosum Complementation Group D Mutant Cell Phenotypes by Chromosome and Gene Transfer: Involvement of the Human ERCC2 DNA Repair Gene

Proceedings of the National Academy of Sciences - PNAS, 1992-01, Vol.89 (1), p.261-265

1992

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A 2.8-Mb Clone Contig of the Multiple Endocrine Neoplasia Type 1 (MEN1) Region at 11q13

Genomics (San Diego, Calif.), 1997-06, Vol.42 (3), p.436-445

1997

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Identification of the inverted chromosome 16 using chromosome painting

British journal of haematology, 1999-03, Vol.104 (3), p.618-620

1999

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A Radiation Hybrid Map of the BRCA1 Region of Chromosome 17q12-q21

Genomics (San Diego, Calif.), 1993-09, Vol.17 (3), p.632-641

1993

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Tetranucleotide repeat polymorphism at D17S846 maps within 40 kb of GAS at 17q12–q22

Human molecular genetics, 1993-07, Vol.2 (7), p.1080-1080

1993

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Localization of the human HTF4 transcription factors 4 gene (TCF12) to chromosome 15q21

Cytogenetic and genome research, 1995-01, Vol.68 (3-4), p.235-238

1995

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A Region of Human Chromosome 9p Required for Testis Development Contains Two Genes Related to Known Sexual Regulators

Human molecular genetics, 1999-06, Vol.8 (6), p.989-996

1999

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Multicolor FISH Mapping with Alu-PCR-Amplified YAC Clone DNA Determines the Order of Markers in the BRCA1 Region on Chromosome 17q12-q21

Genomics (San Diego, Calif.), 1993-09, Vol.17 (3), p.624-631

1993

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Region-specific cosmids and STRPs identified by chromosome microdissection and fish

Genomics (San Diego, Calif.), 1995-01, Vol.25 (2), p.413-420

1995

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Identification and assignment of a new gene (D20S756) to human chromosome 20p13

Cytogenetic and genome research, 1996-01, Vol.73 (4), p.315-316

1996

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Familial breast cancer. Approaching the isolation of a susceptibility gene

Cancer, 1994-08, Vol.74 (S3), p.1013-1020

1994

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Isolation and characterization of somatic cell hybrids with breakpoints spanning 17q22-->q24

Cytogenetic and genome research, 1993-01, Vol.64 (3-4), p.222-223

1993

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Cytogenetic Effects of Phenytoin and/or Carbamazepine on Human Peripheral Leukocytes

Epilepsia (Copenhagen), 1989-05, Vol.30 (3), p.374-379

1989

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Bends in human mitotic metaphase chromosomes, including a bend marking the X-inactivation center

American journal of human genetics, 1984, Vol.36 (1), p.218-226

1984

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A practical metaphase marker of the inactive X chromosome

American journal of human genetics, 1986-07, Vol.39 (1), p.88-95

1986

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Identification of the inverted chromosome 16 using chromosome painting

British journal of haematology, 1999-02, Vol.104 (2), p.201-201

1999

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Location of the X inactivation center in primates and other mammals

Human genetics, 1986-09, Vol.74 (1), p.63-66

1986

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Statistical methods for gene map construction by fluorescence in situ hybridization

Genome research, 1996-12, Vol.6 (12), p.1133-1148

1996

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Familial ring (19) chromosome mosaicism: Case report and review

American journal of medical genetics, 1996-12, Vol.66 (3), p.276-280

1996

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Cytogenetic and molecular analysis of inv dup(15) chromosomes observed in two patients with autistic disorder and mental retardation

American journal of medical genetics, 1996-01, Vol.61 (2), p.182-187

1996

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Chromosome 20 deletion in multiple endocrine neoplasia type 2: Expanded double-blind studies

American journal of medical genetics, 1987-07, Vol.27 (3), p.739-748

1987

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A microfluidics approach for the isolation of nucleated red blood cells (NRBCs) from the peripheral blood of pregnant women

Evidence for a Turner Syndrome Locus or Loci at Xp11.2-p22.1

A Gene Involved in XY Sex Reversal Is Located on Chromosome 9, Distal to Marker D9S1779

Molecular cytogenetic analysis of Inv Dup(15) chromosomes, using probes specific for the Prader-Willi/Angelman syndrome region : clinical implications

Correction of Xeroderma Pigmentosum Complementation Group D Mutant Cell Phenotypes by Chromosome and Gene Transfer: Involvement of the Human ERCC2 DNA Repair Gene

A 2.8-Mb Clone Contig of the Multiple Endocrine Neoplasia Type 1 (MEN1) Region at 11q13

Identification of the inverted chromosome 16 using chromosome painting

A Radiation Hybrid Map of the BRCA1 Region of Chromosome 17q12-q21

Tetranucleotide repeat polymorphism at D17S846 maps within 40 kb of GAS at 17q12–q22

Localization of the human HTF4 transcription factors 4 gene (TCF12) to chromosome 15q21

A Region of Human Chromosome 9p Required for Testis Development Contains Two Genes Related to Known Sexual Regulators

Multicolor FISH Mapping with Alu-PCR-Amplified YAC Clone DNA Determines the Order of Markers in the BRCA1 Region on Chromosome 17q12-q21

Region-specific cosmids and STRPs identified by chromosome microdissection and fish

Identification and assignment of a new gene (D20S756) to human chromosome 20p13

Familial breast cancer. Approaching the isolation of a susceptibility gene

Isolation and characterization of somatic cell hybrids with breakpoints spanning 17q22-->q24

Cytogenetic Effects of Phenytoin and/or Carbamazepine on Human Peripheral Leukocytes

Bends in human mitotic metaphase chromosomes, including a bend marking the X-inactivation center

A practical metaphase marker of the inactive X chromosome

Identification of the inverted chromosome 16 using chromosome painting

Location of the X inactivation center in primates and other mammals

Statistical methods for gene map construction by fluorescence in situ hybridization

Familial ring (19) chromosome mosaicism: Case report and review

Cytogenetic and molecular analysis of inv dup(15) chromosomes observed in two patients with autistic disorder and mental retardation

Chromosome 20 deletion in multiple endocrine neoplasia type 2: Expanded double-blind studies

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