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Gene structure alternative splicing, and chromosomal localization of pro-apoptotic Bcl-2 relative Bim

Mammalian genome, 2001-02, Vol.12 (2), p.163-168

2001

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Characterizing and Mapping Porcine Endogenous Retroviruses in Westran Pigs

Journal of Virology, 2002-06, Vol.76 (11), p.5548-5556

2002

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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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An Orphaned Mammalian β-Globin Gene of Ancient Evolutionary Origin

Proceedings of the National Academy of Sciences - PNAS, 2001-01, Vol.98 (3), p.1101-1106

2001

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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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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.), , Vol.51 (2), p.197-206

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Assignment of the growth hormone receptor gene to band q17 of the homeologous sheep 16 and cattle 20 chromosomes

Mammalian genome, 1998-07, Vol.9 (7), p.599-600

1998

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

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

1999

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Characterization of the EphA1 Receptor Tyrosine Kinase: Expression in Epithelial Tissues

Growth factors (Chur, Switzerland), 2001, Vol.18 (4), p.303-317

2001

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Genomic characterization of the sheep vasopressin V1a receptor gene and promoter, with assignment to bands q23–24 of sheep chromosome 3 and cattle chromosome 5

Gene, 1999-11, Vol.240 (1), p.183-192

1999

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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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Organization and chromosomal localization of the murine Testisin gene encoding a serine protease temporally expressed during spermatogenesis

European journal of biochemistry, 2001-03, Vol.268 (5), p.1250-1258

2001

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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

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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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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KARYOTYPE NOMENCLATURE FOR KNOWN NON-INHERITANCE

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

1972

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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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Gene structure alternative splicing, and chromosomal localization of pro-apoptotic Bcl-2 relative Bim

Characterizing and Mapping Porcine Endogenous Retroviruses in Westran Pigs

Nucleus pulposus cellular longevity by telomerase gene therapy

An Orphaned Mammalian β-Globin Gene of Ancient Evolutionary Origin

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

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)

Assignment of the growth hormone receptor gene to band q17 of the homeologous sheep 16 and cattle 20 chromosomes

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

Characterization of the EphA1 Receptor Tyrosine Kinase: Expression in Epithelial Tissues

Genomic characterization of the sheep vasopressin V1a receptor gene and promoter, with assignment to bands q23–24 of sheep chromosome 3 and cattle chromosome 5

Antisense transcription of a murine FGFR-3 pseudogene duringfetaldevelopment

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

Organization and chromosomal localization of the murine Testisin gene encoding a serine protease temporally expressed during spermatogenesis

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

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

KARYOTYPE NOMENCLATURE FOR KNOWN NON-INHERITANCE

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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