Literature DB >> 21253091

Mendelian genetics.

E Winsor.   

Abstract

The author reviews the inheritance patterns of diseases or conditions caused by genes at a single locus. The recurrence risk in several common family situations is illustrated for autosomal recessive, autosomal dominant, and X-linked inheritance. Patients frequently have difficulty understanding these concepts, and a few examples are provided of problems encountered in genetic counselling.

Entities:  

Year:  1988        PMID： 21253091      PMCID： PMC2218972     

Source DB:  PubMed          Journal:  Can Fam Physician        ISSN： 0008-350X            Impact factor:   3.275


  2 in total

Review 1.  Presumed homozygous achondroplasia. A review and report of a further case.

Authors:  K Aterman; J P Welch; P G Taylor
Journal:  Pathol Res Pract       Date:  1983-08       Impact factor: 3.250

2.  Homozygotes for Huntington's disease.

Authors:  N S Wexler; A B Young; R E Tanzi; H Travers; S Starosta-Rubinstein; J B Penney; S R Snodgrass; I Shoulson; F Gomez; M A Ramos Arroyo
Journal:  Nature       Date:  1987 Mar 12-18       Impact factor: 49.962
  2 in total
  1 in total

1.  Updating genograms in the practice of preventive medicine.

Authors:  P W Allderdice; E O'Leary; S Ficken
Journal:  Can Fam Physician       Date:  1988-04       Impact factor: 3.275
  1 in total

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