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A96 BEST OF PEDIATRICS: Lung Hypoplasia In A Genetic Mouse Model Of Down Syndrome
Rationale: Infants and children with Down syndrome (DS) are at high risk for developing lung hypoplasia and pulmonary hypertension that contributes to cardiorespiratory morbidity and mortality. Genetic mouse models for DS containing mouse orthologues for human chromosome 21 are distributed across th...
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Published in: | American journal of respiratory and critical care medicine 2017-01, Vol.195 |
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container_title | American journal of respiratory and critical care medicine |
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creator | Bush, D Minic, A Seedorf, G Dodson, B Shepherd, D P Abman, S H Galambos, C |
description | Rationale: Infants and children with Down syndrome (DS) are at high risk for developing lung hypoplasia and pulmonary hypertension that contributes to cardiorespiratory morbidity and mortality. Genetic mouse models for DS containing mouse orthologues for human chromosome 21 are distributed across three murine chromosomes, including chromosome 10 (encodes ES) and 16 (encodes RCAN1). |
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Genetic mouse models for DS containing mouse orthologues for human chromosome 21 are distributed across three murine chromosomes, including chromosome 10 (encodes ES) and 16 (encodes RCAN1).</abstract><cop>New York</cop><pub>American Thoracic Society</pub></addata></record> |
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language | eng |
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source | Freely Accessible Journals; EZB Free E-Journals |
subjects | Chromosomes Down syndrome Hypoxia Lungs Pediatrics Rodents |
title | A96 BEST OF PEDIATRICS: Lung Hypoplasia In A Genetic Mouse Model Of Down Syndrome |
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