La variación genética de MSX1 presenta un dimorfismo sexual en la fisura labiopalatina no sindrómica en la población chilena
Background: Recent studies in mice have demonstrated that the Msx-1 homebox gene is implicated in cleft palate. Thus, it has been suggested that its human homologue, MSX1 (HOX-7), located in chromosome 4 could be involved in the etiology of non syndromic cleft lip palate. Aim: To study the linkage b...
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Main Authors: | , , , , |
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Language: | Spanish / Castilian |
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Sociedad Médica de Santiago
1998
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Online Access: | http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0034-98871998000700005 |
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