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Molecular analysis of the APC gene in 205 families: extended genotype-phenotype correlations in FAP and evidence for the role of APC amino acid changes in colorectal cancer predisposition

Journal of medical genetics, 1999-01, Vol.36 (1), p.14-20

1999

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Adenine nucleotide tissue concentrations and liver allograft viability after cold preservation and warm ischemia

Transplantation, 1988-06, Vol.45 (6), p.1016

1988

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Sinusoidal lining cell damage: the critical injury in cold preservation of liver allografts in the rat

Transplantation, 1988-08, Vol.46 (2), p.178

1988

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Close genetic linkage between X-linked retinitis pigmentosa and a restriction fragment length polymorphism identified by recombinant DNA probe L1.28

Nature (London), 1984-05, Vol.309 (5965), p.253-255

1984

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The use of DNA from paraffin wax preserved tissue for predictive diagnosis in familial adenomatous polyposis

Journal of medical genetics, 1992-08, Vol.29 (8), p.571-573

1992

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Genotype-phenotype correlation between position of constitutional APC gene mutation and CHRPE expression in familial adenomatous polyposis

Human genetics, 1994-11, Vol.94 (5), p.543-548

1994

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Prune belly in trisomy 13

Prenatal diagnosis, 1986-09, Vol.6 (5), p.379-382

1986

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Responsibility without guilt: a youngian approach to responsibility for global injustice

McKeown, M C

2015

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Floating-Harbor syndrome

Journal of medical genetics, 1991-03, Vol.28 (3), p.201-204

1991

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De la nordicité au boréalisme

2020

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Southern analysis reveals a large deletion at the hypoxanthine phosphoribosyltransferase locus in a patient with Lesch-Nyhan syndrome

Clinical genetics, 1995-08, Vol.48 (2), p.80-84

1995

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Rapid interphase FISH diagnosis of trisomy 18 on blood smears

The Lancet (British edition), 1992-08, Vol.340 (8817), p.495-495

1992

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Genetic linkage between X-linked retinitis pigmentosa and DNA probe DXS7 {L1.28}: further linkage data, heterogeneity testing, and risk estimation

Human genetics, 1986-10, Vol.74 (2), p.168-171

1986

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Ions and electrons in the electron capture detector : Quantitative identification by atmospheric pressure ionization mass spectrometry

Journal of Chromatography A, 1976-01, Vol.122, p.397-413

1976

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Early Folds and the a -Lineation at Tintagel, Cornwall

Nature (London), 1964-01, Vol.203 (4948), p.933-935

1964

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Increased repair and cell survival in cells treated with DIR1 antisense oligonucleotides: implications for induced radioresistance

International journal of radiation biology, 2000, Vol.76 (5), p.617-623

Robson, M. E. Price, M. L. Moore, M. C. Joiner, V. J. McKelvey-Martin, S. R. McKeown, D. G. Hirst, T.

2000

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Close genetic linkage between X-linked retinitis pigmentosa and a restriction fragment length polymorphism identified by recombinant DNA probe L1.28

Nature (London), 1984-01, Vol.309 (5965), p.253-255

1984

Volltextzugriff (PDF)

Southern analysis reveals a large deletion at the hypoxanthine phosphoribosyltransferase locus in a patients with Lesch-Nyhan syndrome

Clinical genetics, 1995, Vol.48 (2), p.80-84

1995

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Linkage relationships between X-linked retinitis pigmentosa and nine short-arm markers: exclusion of the disease locus from Xp21 and localization to between DXS7 and DXS14

American journal of human genetics, 1987-10, Vol.41 (4), p.635-644

1987

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Submarine examination of lower carboniferous strata on inshore regions of the continental shelf of southeast Scotland

Marine geology, 1969-01, Vol.7 (3), p.235-251

1969

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Transverse-momentum-dependent parton distribution/fragmentation functions at an electron-ion collider

The European physical journal. A, Hadrons and nuclei, 2011-03, Vol.47 (3)

2011

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Role of congenital hypertrophy of the retinal pigment epithelium in the predictive diagnosis of familial

British journal of surgery, 1992, Vol.79 (7), p.689-693

1992

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Linkage relationships between X-linked retinitis pigmentosa and nine-short-arm markers: exclusion of the disease locus from Xp21 and localization to between DX57 and DX514

American journal of human genetics, 1987, Vol.41 (4), p.635-644

1987

Volltextzugriff (PDF)

In situ strain tuning of the metal-insulator-transition of Ca2RuO4 in angle-resolved photoemission experiments

Nature communications, 2018-10, Vol.9 (1), p.1-7, Article 4535

2018

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High-Resolution Photoemission on Sr2RuO4 Reveals Correlation-Enhanced Effective Spin-Orbit Coupling and Dominantly Local Self-Energies

Physical review. X, 2019-06, Vol.9 (2)

2019

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Molecular analysis of the APC gene in 205 families: extended genotype-phenotype correlations in FAP and evidence for the role of APC amino acid changes in colorectal cancer predisposition

Adenine nucleotide tissue concentrations and liver allograft viability after cold preservation and warm ischemia

Sinusoidal lining cell damage: the critical injury in cold preservation of liver allografts in the rat

Close genetic linkage between X-linked retinitis pigmentosa and a restriction fragment length polymorphism identified by recombinant DNA probe L1.28

The use of DNA from paraffin wax preserved tissue for predictive diagnosis in familial adenomatous polyposis

Genotype-phenotype correlation between position of constitutional APC gene mutation and CHRPE expression in familial adenomatous polyposis

Prune belly in trisomy 13

Responsibility without guilt: a youngian approach to responsibility for global injustice

Floating-Harbor syndrome

De la nordicité au boréalisme

Southern analysis reveals a large deletion at the hypoxanthine phosphoribosyltransferase locus in a patient with Lesch-Nyhan syndrome

Rapid interphase FISH diagnosis of trisomy 18 on blood smears

Genetic linkage between X-linked retinitis pigmentosa and DNA probe DXS7 {L1.28}: further linkage data, heterogeneity testing, and risk estimation

Ions and electrons in the electron capture detector : Quantitative identification by atmospheric pressure ionization mass spectrometry

Early Folds and the a -Lineation at Tintagel, Cornwall

Increased repair and cell survival in cells treated with DIR1 antisense oligonucleotides: implications for induced radioresistance

Close genetic linkage between X-linked retinitis pigmentosa and a restriction fragment length polymorphism identified by recombinant DNA probe L1.28

Southern analysis reveals a large deletion at the hypoxanthine phosphoribosyltransferase locus in a patients with Lesch-Nyhan syndrome

Linkage relationships between X-linked retinitis pigmentosa and nine short-arm markers: exclusion of the disease locus from Xp21 and localization to between DXS7 and DXS14

Submarine examination of lower carboniferous strata on inshore regions of the continental shelf of southeast Scotland

Transverse-momentum-dependent parton distribution/fragmentation functions at an electron-ion collider

Role of congenital hypertrophy of the retinal pigment epithelium in the predictive diagnosis of familial

Linkage relationships between X-linked retinitis pigmentosa and nine-short-arm markers: exclusion of the disease locus from Xp21 and localization to between DX57 and DX514

In situ strain tuning of the metal-insulator-transition of Ca2RuO4 in angle-resolved photoemission experiments

High-Resolution Photoemission on Sr2RuO4 Reveals Correlation-Enhanced Effective Spin-Orbit Coupling and Dominantly Local Self-Energies

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