Estudos moleculares em famílias com defeitos de membros

Estudos moleculares em famílias com defeitos de membros

No presente trabalho foram desenvolvidos estudos genético-moleculares em três famílias com três síndromes distintas de defeitos dos membros. A ectrodactilia ou SHFM (split-hand/split-foot malformation) é uma malformação congênita da extremidade dos membros caracterizada por fenda mediana profunda da...

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Bibliographic Details
Main Author:	Aguiar, Renata Soares Thiele de
Other Authors:	Mingroni Netto, Regina Celia
Format:	Others
Language:	pt
Published:	Biblioteca Digitais de Teses e Dissertações da USP 2011
Subjects:	Aplasia fibular Ectrodactilia Ectrodactyly Ectrodactyly with tibial hemimelia Fibular agenesis Genetic Mapping Hemimelia tibial associada à ectrodactilia Mapeamento genético Microssatélites Microssatellite markers SNPs
Online Access:	http://www.teses.usp.br/teses/disponiveis/41/41131/tde-08092011-160454/

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