Compound heterozygous mutations in the IFT140 gene cause Opitz trigonocephaly C syndrome in a patient with typical features of a ciliopathy
C. Peña‐Padilla; C.R. Marshall; S. Walker; S.W. Scherer; G. Tavares‐Macías; G. Razo‐Jiménez; L. Bobadilla‐Morales; E. Acosta‐Fernández; A. Corona‐Rivera; R. Mendoza‐Londono; J. R. Corona‐Rivera
Author Information: Center for Registry and Research on Congenital Anomalies (CRIAC), Division of Pediatrics, Service of Genetics and Cytogenetic Unit
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