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Nucleus pulposus cellular longevity by telomerase gene therapy

Spine (Philadelphia, Pa. 1976), 2007-05, Vol.32 (11), p.1188-1196

2007

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Simultaneous detection of X- and Y-bearing human sperm by double fluorescence in situ hybridization

Molecular reproduction and development, 1993-03, Vol.34 (3), p.308-313

1993

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Antisense transcription of a murine FGFR-3 pseudogene during fetal development

Gene, 1997-03, Vol.187 (1), p.115-122

1997

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Cloning of a human insulin-stimulated protein kinase (ISPK-1) gene and analysis of coding regions and mRNA levels of the ISPK-1 and the protein phosphatase-1 genes in muscle from NIDDM patients

Diabetes (New York, N.Y.), 1995-01, Vol.44 (1), p.90-97

1995

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SOLH, a Human Homologue of theDrosophila melanogaster small optic lobesGene Is a Member of the Calpain and Zinc-Finger Gene Families and Maps to Human Chromosome 16p13.3 nearCATM(Cataract with Microphthalmia)

Genomics (San Diego, Calif.), 1998-07, Vol.51 (2), p.197-206

1998

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Antisense transcription of a murine FGFR-3 pseudogene duringfetaldevelopment

Gene, 1997-03, Vol.187 (1), p.115-122

1997

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Gene structure, expression and chromosomal localization of murine Theta class glutathione transferase mGSTT1-1

Biochemical journal, 1999-01, Vol.337 (1), p.141-151

1999

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Detection of chromosome 17- and X-bearing human spermatozoa using fluorescence in situ hybridization

Molecular reproduction and development, 1992-10, Vol.33 (2), p.189-194

1992

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A fluorescent in situ hybridization analysis of the chromosome constitution of ejaculated sperm in a 47, XYY male

Clinical genetics, 1994-02, Vol.45 (2), p.67-70

1994

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The HumanPIN1Peptidyl-Prolylcis/transIsomerase Gene Maps to Human Chromosome 19p13 and the Closely RelatedPIN1LGene to 1p31

Genomics (San Diego, Calif.), 1997-09, Vol.44 (2), p.157-162

1997

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Chromosomal localization of the human urothelial "tetraspan" gene, UPK1B, to 3q13.3-q21 and detection of a TaqI polymorphism

Genomics (San Diego, Calif.), 1997-03, Vol.40 (3), p.501-503

1997

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Chromosomal Localization of the Human Urothelial “Tetraspan” Gene, UPK1B, to 3q13.3–q21 and Detection of aTaqI Polymorphism

Genomics (San Diego, Calif.), 1997-03, Vol.40 (3), p.501-503

1997

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Retinoblastoma and retinoma occurring in a child with a translocation and deletion of the long arm of chromosome 13

Archives of ophthalmology (1960), 1985-07, Vol.103 (7), p.941-944

1985

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Structure and Chromosomal Localization of the Genomic Locus Encoding theKiz1LIM-Kinase Gene

Genomics (San Diego, Calif.), 1996-08, Vol.35 (3), p.593-596

1996

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Detection of the fragile X chromosome and other fragile sites

Clinical genetics, 1985-05, Vol.27 (5), p.520-521

Webb, Graham C.

1985

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Fragile X testing in a diagnostic cytogenetics laboratory

Journal of medical genetics, 1989-07, Vol.26 (7), p.439-442

1989

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Non C-banding variants in some normal families might be homogeneously staining regions

Human genetics, 1989-04, Vol.82 (1), p.59-62

1989

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TRANSMISSION OF FRAGILE (X) (q27) SITE FROM A MALE

The Lancet (British edition), 1981-11, Vol.318 (8257), p.1231-1232

1981

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A fragile site at 7p11

Pathology, 1983, Vol.15 (1), p.108-109

1983

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CHROMOSOME BANDING REQUIRED FOR STUDIES ON X-LINKED MENTAL RETARDATION

The Lancet (British edition), 1981-01, Vol.317 (8210), p.49-49

1981

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Chromosomal inversions—effects and implications

Pathology, 1983, Vol.15 (1), p.111-112

1983

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Guidelines for the diagnosis of fragile X

Clinical genetics, 1986-02, Vol.29 (2), p.95-95

1986

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KARYOTYPE NOMENCLATURE FOR KNOWN NON-INHERITANCE

The Lancet (British edition), 1972-12, Vol.300 (7791), p.1366-1367

1972

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Duplication of a small segment of 5p due to maternal recombination within a paracentric shift

American journal of medical genetics, 1988-08, Vol.30 (4), p.875-881

1988

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Excess years of life lost to COVID-19 and other causes of death by sex, neighbourhood deprivation, and region in England and Wales during 2020: A registry-based study

PLoS medicine, 2022-02, Vol.19 (2), p.e1003904-e1003904

2022

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Nucleus pulposus cellular longevity by telomerase gene therapy

Simultaneous detection of X- and Y-bearing human sperm by double fluorescence in situ hybridization

Antisense transcription of a murine FGFR-3 pseudogene during fetal development

Cloning of a human insulin-stimulated protein kinase (ISPK-1) gene and analysis of coding regions and mRNA levels of the ISPK-1 and the protein phosphatase-1 genes in muscle from NIDDM patients

SOLH, a Human Homologue of theDrosophila melanogaster small optic lobesGene Is a Member of the Calpain and Zinc-Finger Gene Families and Maps to Human Chromosome 16p13.3 nearCATM(Cataract with Microphthalmia)

Antisense transcription of a murine FGFR-3 pseudogene duringfetaldevelopment

Gene structure, expression and chromosomal localization of murine Theta class glutathione transferase mGSTT1-1

Detection of chromosome 17- and X-bearing human spermatozoa using fluorescence in situ hybridization

A fluorescent in situ hybridization analysis of the chromosome constitution of ejaculated sperm in a 47, XYY male

The HumanPIN1Peptidyl-Prolylcis/transIsomerase Gene Maps to Human Chromosome 19p13 and the Closely RelatedPIN1LGene to 1p31

Chromosomal localization of the human urothelial "tetraspan" gene, UPK1B, to 3q13.3-q21 and detection of a TaqI polymorphism

Chromosomal Localization of the Human Urothelial “Tetraspan” Gene, UPK1B, to 3q13.3–q21 and Detection of aTaqI Polymorphism

Retinoblastoma and retinoma occurring in a child with a translocation and deletion of the long arm of chromosome 13

Structure and Chromosomal Localization of the Genomic Locus Encoding theKiz1LIM-Kinase Gene

Detection of the fragile X chromosome and other fragile sites

Fragile X testing in a diagnostic cytogenetics laboratory

Non C-banding variants in some normal families might be homogeneously staining regions

TRANSMISSION OF FRAGILE (X) (q27) SITE FROM A MALE

A fragile site at 7p11

CHROMOSOME BANDING REQUIRED FOR STUDIES ON X-LINKED MENTAL RETARDATION

Chromosomal inversions—effects and implications

Guidelines for the diagnosis of fragile X

KARYOTYPE NOMENCLATURE FOR KNOWN NON-INHERITANCE

Duplication of a small segment of 5p due to maternal recombination within a paracentric shift

Excess years of life lost to COVID-19 and other causes of death by sex, neighbourhood deprivation, and region in England and Wales during 2020: A registry-based study

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