Literature DB >> 6026586

Testing of single locus hypotheses where there is incomplete separation of the phenotypes.

E A Murphy, D R Bolling.   

Abstract

Mesh:

Substances:

Year:  1967        PMID: 6026586      PMCID: PMC1706272     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


× No keyword cloud information.
  4 in total

1.  ONE CAUSE?MANY CAUSES?THE ARGUMENT FROM THE BIMODAL DISTRIBUTION.

Authors:  E A MURPHY
Journal:  J Chronic Dis       Date:  1964-04

2.  Heredity in hypertension.

Authors:  R PLATT
Journal:  Lancet       Date:  1963-04-27       Impact factor: 79.321

3.  Further observations on the determination of the isoniazid inactivator phenotype.

Authors:  D A EVANS; P B STOREY; V A McKUSICK
Journal:  Bull Johns Hopkins Hosp       Date:  1961-01

4.  The pseudocholinesterase variants. Esterase levels and dibucaine numbers in families selected through suxamethonium sensitive individuals.

Authors:  H HARRIS; M WHITTAKER; H LEHMANN; E SILK
Journal:  Acta Genet Stat Med       Date:  1960
  4 in total
  10 in total

1.  General models for segregation analysis.

Authors:  R C Elston; K C Yelverton
Journal:  Am J Hum Genet       Date:  1975-01       Impact factor: 11.025

2.  Diagnosing familial hypercholesterolaemia in childhood by measuring serum cholesterol.

Authors:  J V Leonard; A G Whitelaw; O H Wolff; J K Lloyd; J Slack
Journal:  Br Med J       Date:  1977-06-18

3.  Testing for bimodality in frequency distributions of data suggesting polymorphisms of drug metabolism--hypothesis testing.

Authors:  P R Jackson; G T Tucker; H F Woods
Journal:  Br J Clin Pharmacol       Date:  1989-12       Impact factor: 4.335

4.  Deduction, inference and illation.

Authors:  E A Murphy; E M Rosell; M I Rosell
Journal:  Theor Med       Date:  1986-10

5.  Genetic aspects of the polymodally distributed sulphoxidation of S-carboxymethyl-L-cysteine in man.

Authors:  S C Mitchell; R H Waring; C S Haley; J R Idle; R L Smith
Journal:  Br J Clin Pharmacol       Date:  1984-10       Impact factor: 4.335

6.  Some difficulties in the investigation of genetic factors in coronary artery disease.

Authors:  E A Murphy
Journal:  Can Med Assoc J       Date:  1967-11-11       Impact factor: 8.262

7.  Hyperlipidemia in coronary heart disease. II. Genetic analysis of lipid levels in 176 families and delineation of a new inherited disorder, combined hyperlipidemia.

Authors:  J L Goldstein; H G Schrott; W R Hazzard; E L Bierman; A G Motulsky
Journal:  J Clin Invest       Date:  1973-07       Impact factor: 14.808

8.  The genetic control of sparteine and debrisoquine metabolism in man with new methods of analysing bimodal distributions.

Authors:  D A Evans; D Harmer; D Y Downham; E J Whibley; J R Idle; J Ritchie; R L Smith
Journal:  J Med Genet       Date:  1983-10       Impact factor: 6.318

9.  Familial hypercholesterolemia (one form of familial type II hyperlipoproteinemia). A study of its biochemical, genetic and clinical presentation in childhood.

Authors:  P O Kwiterovich; D S Fredrickson; R I Levy
Journal:  J Clin Invest       Date:  1974-05       Impact factor: 14.808

10.  Genotyping and inflated type I error rate in genome-wide association case/control studies.

Authors:  Joshua N Sampson; Hongyu Zhao
Journal:  BMC Bioinformatics       Date:  2009-02-23       Impact factor: 3.169

  10 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.