Author: Florence G. Blake
Publisher:
ISBN:
Category : Babysitters
Languages : en
Pages : 704
Book Description
Phenylketonuria Detection in the Newborn Infant as a Routine Hospital Procedure
Author: Florence G. Blake
Publisher:
ISBN:
Category : Babysitters
Languages : en
Pages : 704
Book Description
Publisher:
ISBN:
Category : Babysitters
Languages : en
Pages : 704
Book Description
Phenylketonuria Detection in the Newborn Infant as a Routine Hospital Procedure
Author: Robert Guthrie
Publisher:
ISBN:
Category : Child welfare
Languages : en
Pages : 88
Book Description
Publisher:
ISBN:
Category : Child welfare
Languages : en
Pages : 88
Book Description
Bureau Publication
Author: Robert Guthrie
Publisher:
ISBN:
Category : Child welfare
Languages : en
Pages : 73
Book Description
Publisher:
ISBN:
Category : Child welfare
Languages : en
Pages : 73
Book Description
Phenylketonuria Detection in the Newborn Infant as a Routine Hospital Procedure
Author:
Publisher:
ISBN:
Category : Heart
Languages : en
Pages : 102
Book Description
Publisher:
ISBN:
Category : Heart
Languages : en
Pages : 102
Book Description
Phenylketonuria Detection in the Newborn Infant as a Routine Hospital Procedure
Author: Robert Guthrie
Publisher:
ISBN:
Category : Metabolism
Languages : en
Pages : 84
Book Description
Publisher:
ISBN:
Category : Metabolism
Languages : en
Pages : 84
Book Description
Phenylketonuria Detection in the Newborn Infant as a Routine Hospital Procedure
Author: Robert Guthrie
Publisher:
ISBN:
Category : Infants
Languages : en
Pages : 82
Book Description
Publisher:
ISBN:
Category : Infants
Languages : en
Pages : 82
Book Description
Newborn Screening for Genetic-metabolic Diseases
Author: Neil Anton Holtzman
Publisher:
ISBN:
Category : Genetic screening
Languages : en
Pages : 32
Book Description
Publisher:
ISBN:
Category : Genetic screening
Languages : en
Pages : 32
Book Description
Recommended Guidelines for PKU Programs for the Newborn
Author: United States. Maternal and Child Health Service
Publisher:
ISBN:
Category : Phenylketonuria
Languages : en
Pages : 20
Book Description
Publisher:
ISBN:
Category : Phenylketonuria
Languages : en
Pages : 20
Book Description
Management of Newborn Infants with Phenylketonuria
Author: United States. Health Services Administration. Bureau of Community Health Services
Publisher:
ISBN:
Category : Children
Languages : en
Pages : 48
Book Description
Publisher:
ISBN:
Category : Children
Languages : en
Pages : 48
Book Description
Moments of Truth in Genetic Medicine
Author: M. Susan Lindee
Publisher: JHU Press
ISBN: 080189915X
Category : Medical
Languages : en
Pages : 283
Book Description
Genetic research increasingly dominates medical thought and practice in the United States and in many other industrialized nations. Susan Lindee's original study explores the institutions, disciplines, and ideas that initiated the reconfiguration of genetic medicine from a marginal field in the mid-1950s to a core research frontier of biomedicine. Tracing the work of geneticists and other experts in identifying and classifying disease during the explosive period between 1950 and 1980, Lindee identifies the individual "moments of truth" that moved the field away from its eugenic past to the center of a new world view in which nearly all disease is understood to be fundamentally genetic. She suggests that these moments of truth were experienced not only by scientists but also by those who had familial, intimate, emotional knowledge of hereditary disease: patients, family members, and research subjects. Focusing on benchmarks in the field—such as the rise of neonatal testing in the 1960s, genetic studies of unique human populations such as the Amish, the development of human cytogenetics and human behavioral genetics, and the efforts to find genes for rare diseases such as familial dysautonomia—she tracks the emergence of a biomedical consensus that nearly all disease is genetic disease. Using the success of this field as a point of entry, Lindee chronicles both the production of knowledge in biomedicine and changes in the cultural meaning of the body in the late twentieth century. She suggests that scientific knowledge is a community project that is shaped directly by people in many different social and professional locations. The power to experience and report scientific truth may be much more dispersed than it sometimes appears, because people know things about their own bodies, and their knowledge has often been incorporated into the technical infrastructure of genomic medicine. Lindee's pathbreaking study shows the interdependence of technical and social parameters in contemporary biomedicine.
Publisher: JHU Press
ISBN: 080189915X
Category : Medical
Languages : en
Pages : 283
Book Description
Genetic research increasingly dominates medical thought and practice in the United States and in many other industrialized nations. Susan Lindee's original study explores the institutions, disciplines, and ideas that initiated the reconfiguration of genetic medicine from a marginal field in the mid-1950s to a core research frontier of biomedicine. Tracing the work of geneticists and other experts in identifying and classifying disease during the explosive period between 1950 and 1980, Lindee identifies the individual "moments of truth" that moved the field away from its eugenic past to the center of a new world view in which nearly all disease is understood to be fundamentally genetic. She suggests that these moments of truth were experienced not only by scientists but also by those who had familial, intimate, emotional knowledge of hereditary disease: patients, family members, and research subjects. Focusing on benchmarks in the field—such as the rise of neonatal testing in the 1960s, genetic studies of unique human populations such as the Amish, the development of human cytogenetics and human behavioral genetics, and the efforts to find genes for rare diseases such as familial dysautonomia—she tracks the emergence of a biomedical consensus that nearly all disease is genetic disease. Using the success of this field as a point of entry, Lindee chronicles both the production of knowledge in biomedicine and changes in the cultural meaning of the body in the late twentieth century. She suggests that scientific knowledge is a community project that is shaped directly by people in many different social and professional locations. The power to experience and report scientific truth may be much more dispersed than it sometimes appears, because people know things about their own bodies, and their knowledge has often been incorporated into the technical infrastructure of genomic medicine. Lindee's pathbreaking study shows the interdependence of technical and social parameters in contemporary biomedicine.