Literature DB >> 15735957

Julia Bell and the Treasury of Human Inheritance.

Peter S Harper1.   

Abstract

The Treasury of Human Inheritance represents the most extensive, and one of the earliest series of documentations and analyses of human genetic disorders. Published between 1909 and 1958, from The Galton Laboratory, London, most of the numerous sections were written by Julia Bell, who represents a key figure in the development of human and medical genetics. Her combination of mathematical training, genetic knowledge and clinical expertise yielded numerous important insights into human inheritance first appearing in the Treasury; it remains a valuable scientific as well as an historical record of the genetics of a range of important inherited disorders.

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Year:  2005        PMID: 15735957     DOI: 10.1007/s00439-005-1264-5

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  9 in total

1.  Nettleship, Pearson and Bateson: the biometric-Mendelian debate in a medical context.

Authors:  A R Rushton
Journal:  J Hist Med Allied Sci       Date:  2000-04       Impact factor: 2.088

2.  Dystrophia myotonica in childhood.

Authors:  T M VANIER
Journal:  Br Med J       Date:  1960-10-29

3.  Julia Bell (1879-1979). Steamboat Lady, statistician and geneticist.

Authors:  S Bundey
Journal:  J Med Biogr       Date:  1996-02

4.  The problem of anticipation in pedigrees of dystrophia myotonica.

Authors:  L S PENROSE
Journal:  Ann Eugen       Date:  1948-04

5.  Anticipation in myotonic dystrophy: fact or fiction?

Authors:  C J Höweler; H F Busch; J P Geraedts; M F Niermeijer; A Staal
Journal:  Brain       Date:  1989-06       Impact factor: 13.501

6.  Linkage in a family with X-linked Charcot-Marie-Tooth disease.

Authors:  N Haites; N Fairweather; C Clark; K F Kelly; S Simpson; A W Johnston
Journal:  Clin Genet       Date:  1989-06       Impact factor: 4.438

7.  Anticipation in myotonic dystrophy: new light on an old problem.

Authors:  P S Harper; H G Harley; W Reardon; D J Shaw
Journal:  Am J Hum Genet       Date:  1992-07       Impact factor: 11.025

8.  Influence of sex of the transmitting parent as well as of parental allele size on the CTG expansion in myotonic dystrophy (DM).

Authors:  H G Brunner; H T Brüggenwirth; W Nillesen; G Jansen; B C Hamel; R L Hoppe; C E de Die; C J Höweler; B A van Oost; B Wieringa
Journal:  Am J Hum Genet       Date:  1993-11       Impact factor: 11.025

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

Authors:  H G Harley; J D Brook; S A Rundle; S Crow; W Reardon; A J Buckler; P S Harper; D E Housman; D J Shaw
Journal:  Nature       Date:  1992-02-06       Impact factor: 49.962

  9 in total
  5 in total

1.  Linkage methods in human genetics before the computer.

Authors:  A W F Edwards
Journal:  Hum Genet       Date:  2005-12       Impact factor: 4.132

2.  William Bateson, human genetics and medicine.

Authors:  Peter S Harper
Journal:  Hum Genet       Date:  2005-10       Impact factor: 4.132

3.  Wilhelm Weinberg's early contribution to segregation analysis.

Authors:  Alan Stark; Eugene Seneta
Journal:  Genetics       Date:  2013-09       Impact factor: 4.562

Review 4.  Human genetics in troubled times and places.

Authors:  Peter S Harper
Journal:  Hereditas       Date:  2017-08-03       Impact factor: 3.271

Review 5.  ADAMTS-12: a multifaced metalloproteinase in arthritis and inflammation.

Authors:  Jianlu Wei; Brendon Richbourgh; Tanghong Jia; Chuanju Liu
Journal:  Mediators Inflamm       Date:  2014-04-28       Impact factor: 4.711

  5 in total

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