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Title Exploring human heredity
Subject Heredity, Human; Medical genetics; Adaptation (Biology)
Description Twentieth Annual Frederick William Reynolds Lecture.
Creator Stephens, Fayette Ellsworth, 1890-
Publisher Extension Division, University of Utah
Date 1956-01-16
Date Digital 2008-05-29
Type Text
Format image/jpeg
Digitization Specifications Original scanned on Epson Expression 10000XL flatbed scanner and saved as 400 ppi uncompressed tiff. Display images generated in PhotoshopCS and uploaded into CONTENTdm Aquisition Station.
Resource Identifier http://content.lib.utah.edu/u?/reynolds,362
Source LD5526 .U8 n.s. v.47 no.11
Language eng
Relation Digital reproduction of "Exploring human heredity" J. Willard Marriott Library Special Collections
Rights Digital Image Copyright University of Utah
Metadata Cataloger Seungkeol Choe; Ken Rockwell
ARK ark:/87278/s64q7rxv
Setname uu_fwrl
Date Created 2008-07-29
Date Modified 2008-07-31
ID 319670
Reference URL https://collections.lib.utah.edu/ark:/87278/s64q7rxv

Page Metadata

Title Page18
Description 18 TWENTIETH ANNUAL REYNOLDS LECTURE Fi gure 5 shows an individual affected with this type of dystrophy, and Figures 6 and 7 show a pedigree history of a large kindred showing the same trait. It has taken many years to accumulate this data. Our policy has been to communicate personally with every available member of the kindred and to provide for an examination by the clinician whenever possible. Almost without exception members of the kindred have been cooperative and helpful. This is but one of over a dozen unrelated kindreds showing the same trait on which we have taken data. Of the 1,249 individuals considered in this kindred, 159 are known to have had muscular dystrophy. The inheritance is that of a Mendelian dominant. A kindred of this type is valuable not only because it provides large numbers and makes the genetic pattern easier to determine, but it makes diagnosis easier for the physician. It gives him an opportunity to see the disease in all of its different forms of expression. Because of this he is able to detect and identify isolated cases of varying degrees of expression. Tyler, F. H., and Stephens, F. E. 1950. Annals of Internal Medicine 32 (4): 640-660. Figure 5
Format image/jpeg
Identifier 018-RNLT-StephensF_Page18.jpg
Source Original Manuscript:Exploring human heredity by Fayette E. Stephens.
Setname uu_fwrl
Date Created 2008-07-29
Date Modified 2008-07-29
ID 319652
Reference URL https://collections.lib.utah.edu/ark:/87278/s64q7rxv/319652