We have presented a family in which three children (1 male and 2 females) who had two different fathers were affected with the Pierre Robin anomalad. The mother exhibits some of the characteristic stigmata of this syndrome which strongly suggests that an autosomal dominant from of the Pierre Robin anomalad exists with variable expressivity
As anomalias congênitas afetam mundialmente cerca de 5% dos nascidos vivos, dentre as quais as alter...
A wide spectrum of anomalies can be associated with Pierre Robin sequence. This report presents a 3-...
We present a family segregating for an autosomal dominant syndrome of hypotelorism, cleft palate/uvu...
Pierre Robin anomalad is a syndrome characterized by cleft of the palate, micrognathia of the mandib...
Pierre Robin syndrome is characterized by micrognathia, glossoptosis and palatal malformation. We re...
New born babies could suffer from multiple craniofacial abnormalities, such as Pierre Robin syndrome...
Abstract The Pierre Robin Syndrome (PRS) consists of a triad of anomalies characterized by micrognat...
© 2015 Jessie Xin XuBackground Pierre Robin Sequence (PRS) is a common craniofacial anomaly compri...
© 2004 BMJ Publishing Group LimitedRobin sequence (RS) is a developmental anomaly characterised by m...
SUMMARY A second family is described in which camptodactyly, club foot, and cleft palate (the Gordon...
When Pierre Robin sequence is associated with many congenital abnormalities, prompt diagnosis and tr...
The systematic investigations on genealogical data of children with clefts have revealed that there ...
The Pierre Robin sequence (PRS) is the nonrandom association of micrognathia, cleft palate, and glos...
We report on a Brazilian mother and her son affected with mandibulofacial dysostosis, growth and men...
Background: The Pierre Robin sequence (PRS), consisting of cleft palate, micrognathia and glossoptos...
As anomalias congênitas afetam mundialmente cerca de 5% dos nascidos vivos, dentre as quais as alter...
A wide spectrum of anomalies can be associated with Pierre Robin sequence. This report presents a 3-...
We present a family segregating for an autosomal dominant syndrome of hypotelorism, cleft palate/uvu...
Pierre Robin anomalad is a syndrome characterized by cleft of the palate, micrognathia of the mandib...
Pierre Robin syndrome is characterized by micrognathia, glossoptosis and palatal malformation. We re...
New born babies could suffer from multiple craniofacial abnormalities, such as Pierre Robin syndrome...
Abstract The Pierre Robin Syndrome (PRS) consists of a triad of anomalies characterized by micrognat...
© 2015 Jessie Xin XuBackground Pierre Robin Sequence (PRS) is a common craniofacial anomaly compri...
© 2004 BMJ Publishing Group LimitedRobin sequence (RS) is a developmental anomaly characterised by m...
SUMMARY A second family is described in which camptodactyly, club foot, and cleft palate (the Gordon...
When Pierre Robin sequence is associated with many congenital abnormalities, prompt diagnosis and tr...
The systematic investigations on genealogical data of children with clefts have revealed that there ...
The Pierre Robin sequence (PRS) is the nonrandom association of micrognathia, cleft palate, and glos...
We report on a Brazilian mother and her son affected with mandibulofacial dysostosis, growth and men...
Background: The Pierre Robin sequence (PRS), consisting of cleft palate, micrognathia and glossoptos...
As anomalias congênitas afetam mundialmente cerca de 5% dos nascidos vivos, dentre as quais as alter...
A wide spectrum of anomalies can be associated with Pierre Robin sequence. This report presents a 3-...
We present a family segregating for an autosomal dominant syndrome of hypotelorism, cleft palate/uvu...