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HEREDITARY ACHONDROPLASIA IN THE RABBIT : I. PHYSICAL APPEARANCE AND GENERAL FEATURES

An achondroplastic condition in the rabbit has been described. It is present at birth and is characterized by size reduction, by a disproportion of bodily parts, most marked in the extremities, and by an invariably lethal effect. The animals are still-born or die very shortly after birth. In physica...

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Detalles Bibliográficos
Autores principales: Brown, Wade H., Pearce, Louise
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1945
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2135558/
https://www.ncbi.nlm.nih.gov/pubmed/19871498
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author Brown, Wade H.
Pearce, Louise
author_facet Brown, Wade H.
Pearce, Louise
author_sort Brown, Wade H.
collection PubMed
description An achondroplastic condition in the rabbit has been described. It is present at birth and is characterized by size reduction, by a disproportion of bodily parts, most marked in the extremities, and by an invariably lethal effect. The animals are still-born or die very shortly after birth. In physical appearance and in the character of the skeletal changes as shown by x-ray photographs, achondroplasia in the rabbit has a remarkable resemblance to the disease in man and in cattle and dogs. The condition which first occurred in offspring of pure bred Havana rabbits is inherited. In anticipation of the later discussion of this phase of the study (13), it can be stated that the mode of inheritance is on the basis of a simple recessive unit factor and that the appearance of non-achondroplastic transmitters (heterozygotes) is that of normal animals.
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spelling pubmed-21355582008-04-18 HEREDITARY ACHONDROPLASIA IN THE RABBIT : I. PHYSICAL APPEARANCE AND GENERAL FEATURES Brown, Wade H. Pearce, Louise J Exp Med Article An achondroplastic condition in the rabbit has been described. It is present at birth and is characterized by size reduction, by a disproportion of bodily parts, most marked in the extremities, and by an invariably lethal effect. The animals are still-born or die very shortly after birth. In physical appearance and in the character of the skeletal changes as shown by x-ray photographs, achondroplasia in the rabbit has a remarkable resemblance to the disease in man and in cattle and dogs. The condition which first occurred in offspring of pure bred Havana rabbits is inherited. In anticipation of the later discussion of this phase of the study (13), it can be stated that the mode of inheritance is on the basis of a simple recessive unit factor and that the appearance of non-achondroplastic transmitters (heterozygotes) is that of normal animals. The Rockefeller University Press 1945-09-30 /pmc/articles/PMC2135558/ /pubmed/19871498 Text en Copyright © Copyright, 1945, by The Rockefeller Institute for Medical Research New York This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Article
Brown, Wade H.
Pearce, Louise
HEREDITARY ACHONDROPLASIA IN THE RABBIT : I. PHYSICAL APPEARANCE AND GENERAL FEATURES
title HEREDITARY ACHONDROPLASIA IN THE RABBIT : I. PHYSICAL APPEARANCE AND GENERAL FEATURES
title_full HEREDITARY ACHONDROPLASIA IN THE RABBIT : I. PHYSICAL APPEARANCE AND GENERAL FEATURES
title_fullStr HEREDITARY ACHONDROPLASIA IN THE RABBIT : I. PHYSICAL APPEARANCE AND GENERAL FEATURES
title_full_unstemmed HEREDITARY ACHONDROPLASIA IN THE RABBIT : I. PHYSICAL APPEARANCE AND GENERAL FEATURES
title_short HEREDITARY ACHONDROPLASIA IN THE RABBIT : I. PHYSICAL APPEARANCE AND GENERAL FEATURES
title_sort hereditary achondroplasia in the rabbit : i. physical appearance and general features
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2135558/
https://www.ncbi.nlm.nih.gov/pubmed/19871498
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