Holocardio amorfo mielocéfalo
Liens Garlobo, Inmaculada; Peña Reyes, Justo Moisés; Gómez Pérez, Humberto; Pons Porrata, Laura María.
Medisan
; 11(3)jul.-sept. 2007. ilus
Artículo en Español | CUMED | ID: cum-35503
Documentos relacionados
[Clinical phenotype and genetic analysis of a fetus with recombinant chromosome 8 syndrome].
Contribution of single-gene defects to congenital cardiac left-sided lesions in the prenatal setting.
Trust in prenatal exome sequencing for expectant families facing unexplained fetal anomalies.
Report of new variants in PPIL1 underlying type 14 pontocerebellar hypoplasia and their associated phenotypic manifestations in two fetuses.
[Prenatal diagnosis of fetuses with renal anomalies by whole genome sequencing].
Diagnostic yield of exome sequencing in fetuses with multisystem malformations: systematic review and meta-analysis.
Diagnostic yield and psychological outcomes among women pursuing trio-exome sequencing: Do women with recurrent anomalous fetal phenotypes experience more negative psychological outcomes?
Duplicated distal phalanx of thumb or hallux in trisomy 13: A recurrent feature in a series of 42 fetuses.
Absent Pulmonary Valve Syndrome in a Fetus: A Case Report and Literature Review.
Information is power: The experiences, attitudes and needs of individuals who chose to have prenatal genomic sequencing for fetal anomalies.