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Human genetics in troubled times and places

Hereditas, 2018, Vol.155 (1), p.7-14, Article 7

Harper, Peter S

2018

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History of Human Genetics: Aspects of Its Development and Global Perspectives

1, 2017

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Mixed Blessings from a Cambridge Union, Elizabeth N Anionwu: 2016. London: ELIZAN. ISBN 978-0-9955268-0-8

Human Genetics, 2018-12, Vol.137 (11-12), p.973-973

Harper, Peter S.

2018

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Recorded interviews with human and medical geneticists

Human genetics, 2017-02, Vol.136 (2), p.149-164

Harper, Peter S.

2017

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The European Society of Human Genetics: beginnings, early history and development over its first 25 years

European journal of human genetics : EJHG, 2017-05

Harper, Peter S

2017

Volltextzugriff (PDF)

Some pioneers of European human genetics

European journal of human genetics : EJHG, 2017-05

Harper, Peter S

2017

Volltextzugriff (PDF)

Activities and initiatives of the renewed European Society of Human Genetics (ESHG) (1992-2017)

European journal of human genetics : EJHG, 2017-12, Vol.25 (s2), p.S2-S5

Harper, Peter S

2017

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Lysenko and Russian genetics: Reply to Wang &Liu

European journal of human genetics : EJHG, 2017-10, Vol.25 (10), p.1098-1098

Harper, Peter S

2017

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Mary Lyon and the hypothesis of random X chromosome inactivation

Human genetics, 2011-08, Vol.130 (2), p.169-174

Harper, Peter S.

2011

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The Evolution of Medical Genetics: A British Perspective

Harper, Peter

1st edition., 2019

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F. Burkhardt et al. (eds.): The correspondence of Charles Darwin: Volume 20, 1872, Cambridge University Press, Cambridge, 2013

Human Genetics, 2014-03, Vol.133 (3), p.379-380

Harper, Peter S.

2014

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Bayes’ rule, medical genetics and the wider world. A review of: the theory that would not die. How Bayes’ rule cracked the Enigma code, hunted down Russian submarines, and emerged triumphant from two centuries of controversy: by Sharon Bertsch McGrayne: New Haven, Yale University Press (2011; revised paperback edition 2012)

Human Genetics, 2013-12, Vol.132 (12), p.1433-1435

Harper, Peter S.

2013

Volltextzugriff (PDF)

Early medical genetics in Soviet Russia: its growth and destruction: A review of ‘The Dawn of Human Genetics’ by V.V. Babkov. Cold Spring Harbor Laboratory Press. 2013

Human Genetics, 2013-10, Vol.132 (10), p.1193-1196

Harper, Peter S.

2013

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Harper's Practical Genetic Counselling

8, 2020

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Relationship between trinucleotide repeat expansion and phenotypic variation in Huntington's disease

Nature genetics, 1993-08, Vol.4 (4), p.393-397

1993

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Expansion of an unstable DNA region and phenotypic variation in myotonic dystrophy

Nature (London), 1992-02, Vol.355 (6360), p.545-546

1992

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Rebecca Skloot: The immortal life of Henrietta Lacks: Crown, SB, 384 pages, ISBN 978-1400052172

Human Genetics, 2011-04, Vol.129 (4), p.463-464

Harper, Peter S.

2011

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Fiftieth anniversary of trisomy 21: returning to a discovery

Human genetics, 2009-08, Vol.126 (2), p.317-324

2009

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Jones S, Keynes M (eds): Twelve Galton lectures. A centenary selection with commentaries: The Galton Institute, 2007, 348 pages, Price £5, Hardback ISBN 978-0-9546570-1-7

Human Genetics, 2010-03, Vol.127 (3), p.371-372

Harper, Peter S.

2010

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Naming of syndromes and unethical activities: the case of Hallervorden and Spatz

The Lancet (British edition), 1996-11, Vol.348 (9036), p.1224-1225

Harper, Peter S

1996

Volltextzugriff (PDF)

Aberrant Interactions of Transcriptional Repressor Proteins with the Huntington's Disease Gene Product, Huntingtin

Human molecular genetics, 1999-09, Vol.8 (9), p.1647-1655

1999

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The discovery of the human chromosome number in Lund, 1955-1956

Human genetics, 2006-03, Vol.119 (1-2), p.226-232

HARPER, Peter S

2006

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Ten years of presymptomatic testing for Huntington's disease: the experience of the UK Huntington's Disease Prediction Consortium

Journal of medical genetics, 2000-08, Vol.37 (8), p.567-571

2000

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Paul Polani and the development of medical genetics

Human genetics, 2007-01, Vol.120 (5), p.723-731

HARPER, Peter S

2007

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Human genetics in troubled times and places

History of Human Genetics: Aspects of Its Development and Global Perspectives

Mixed Blessings from a Cambridge Union, Elizabeth N Anionwu: 2016. London: ELIZAN. ISBN 978-0-9955268-0-8

Recorded interviews with human and medical geneticists

The European Society of Human Genetics: beginnings, early history and development over its first 25 years

Some pioneers of European human genetics

Activities and initiatives of the renewed European Society of Human Genetics (ESHG) (1992-2017)

Lysenko and Russian genetics: Reply to Wang &Liu

Mary Lyon and the hypothesis of random X chromosome inactivation

The Evolution of Medical Genetics: A British Perspective

F. Burkhardt et al. (eds.): The correspondence of Charles Darwin: Volume 20, 1872, Cambridge University Press, Cambridge, 2013

Early medical genetics in Soviet Russia: its growth and destruction: A review of ‘The Dawn of Human Genetics’ by V.V. Babkov. Cold Spring Harbor Laboratory Press. 2013

Harper's Practical Genetic Counselling

Relationship between trinucleotide repeat expansion and phenotypic variation in Huntington's disease

Expansion of an unstable DNA region and phenotypic variation in myotonic dystrophy

Rebecca Skloot: The immortal life of Henrietta Lacks: Crown, SB, 384 pages, ISBN 978-1400052172

Fiftieth anniversary of trisomy 21: returning to a discovery

Jones S, Keynes M (eds): Twelve Galton lectures. A centenary selection with commentaries: The Galton Institute, 2007, 348 pages, Price £5, Hardback ISBN 978-0-9546570-1-7

Naming of syndromes and unethical activities: the case of Hallervorden and Spatz

Aberrant Interactions of Transcriptional Repressor Proteins with the Huntington's Disease Gene Product, Huntingtin

The discovery of the human chromosome number in Lund, 1955-1956

Confirmation of the Type 2 Myotonic Dystrophy (CCTG) n Expansion Mutation in Patients with Proximal Myotonic Myopathy/Proximal Myotonic Dystrophy of Different European Origins: A Single Shared Haplotype Indicates an Ancestral Founder Effect

Ten years of presymptomatic testing for Huntington's disease: the experience of the UK Huntington's Disease Prediction Consortium

Paul Polani and the development of medical genetics

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