Molecular screening for microdeletions at 9p22-p24 and 11q23-q24 in a large cohort of patients with trigonocephaly.

Molecular screening for microdeletions at 9p22-p24 and 11q23-q24 in a large cohort of patients with trigonocephaly.

Trigonocephaly is a rare form of craniosynostosis characterized by the premature closure of the metopic suture. To contribute to a better understanding of the genetic basis of metopic synostosis and in an attempt to restrict the candidate regions related to metopic suture fusion, we studied 76 unrel...

Podrobná bibliografie
Hlavní autoři:	Jehee, F, Johnson, D, Alonso, L, Cavalcanti, D, de Sá Moreira, E, Alberto, F, Kok, F, Kim, C, Wall, SA, Jabs, E, Boyadjiev, SA, Wilkie, A, Passos-Bueno, MR
Médium:	Journal article
Jazyk:	English
Vydáno:	2005

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