[[abstract]]Counseling parents of a fetus with trisomy 13 mosaicism remains difficult because of the phenotypic variability associated with the condition; some patients exhibit the typical phenotype of complete trisomy 13 with neonatal death, while others have few dysmorphic features and prolonged survival. This article provides a comprehensive review of the prenatal diagnosis and genetic counseling for mosaic trisomy 13, including confined placental mosaicism 13, mosaic trisomy 13 diagnosed at amniocentesis, and phylloid hypomelanosis in association with mosaic trisomy 13
[[abstract]]Objective To present prenatal diagnosis and molecular genetic analyses of mosaic trisomy...
Objective To present prenatal diagnosis and molecular genetic analyses of mosaic trisomy 7 Materials...
Mosaic trisomy 13 is estimated to occur in 5% of all trisomy 13 cases. Presentation of trisomy 13 mo...
AbstractCounseling parents of a fetus with trisomy 13 mosaicism remains difficult because of the phe...
Phenotypic outcome and clinical effect of mosaic of trisomy 13 is not clear yet. Eventhough, there i...
Objective: We present prenatal diagnosis of low-level mosaicism for trisomy 13 at amniocentesis asso...
Prenatally detected chromosomal mosaicism complicates genetic counseling as there is variability in ...
Objective: We present prenatal diagnosis of recurrent mosaic ring chromosome 13 [r(13)] of maternal ...
There are currently limited data describing the natural history and outcome for fetal trisomy 13 dia...
Complete Trisomy 13 or Patau’s Syndrome is a relatively common (1/10,000 births) and uniformly fatal...
[[abstract]]Objective: Prenatal diagnosis of mos45,X/46,X,+mar is difficult in genetic counseling. P...
Background Trisomy 13 occurs in 1/10 000e20 000 live births, and mosaicism accounts for 5 % of these...
The identification of trisomy mosaicism in the prenatal setting is often shrouded with uncertainty f...
Introduction: Orofacial clefts are important congenital malformations of the lip, palate, or both ca...
Objective: We present prenatal diagnosis of mosaic trisomy 18 and maternal uniparental disomy (UPD) ...
[[abstract]]Objective To present prenatal diagnosis and molecular genetic analyses of mosaic trisomy...
Objective To present prenatal diagnosis and molecular genetic analyses of mosaic trisomy 7 Materials...
Mosaic trisomy 13 is estimated to occur in 5% of all trisomy 13 cases. Presentation of trisomy 13 mo...
AbstractCounseling parents of a fetus with trisomy 13 mosaicism remains difficult because of the phe...
Phenotypic outcome and clinical effect of mosaic of trisomy 13 is not clear yet. Eventhough, there i...
Objective: We present prenatal diagnosis of low-level mosaicism for trisomy 13 at amniocentesis asso...
Prenatally detected chromosomal mosaicism complicates genetic counseling as there is variability in ...
Objective: We present prenatal diagnosis of recurrent mosaic ring chromosome 13 [r(13)] of maternal ...
There are currently limited data describing the natural history and outcome for fetal trisomy 13 dia...
Complete Trisomy 13 or Patau’s Syndrome is a relatively common (1/10,000 births) and uniformly fatal...
[[abstract]]Objective: Prenatal diagnosis of mos45,X/46,X,+mar is difficult in genetic counseling. P...
Background Trisomy 13 occurs in 1/10 000e20 000 live births, and mosaicism accounts for 5 % of these...
The identification of trisomy mosaicism in the prenatal setting is often shrouded with uncertainty f...
Introduction: Orofacial clefts are important congenital malformations of the lip, palate, or both ca...
Objective: We present prenatal diagnosis of mosaic trisomy 18 and maternal uniparental disomy (UPD) ...
[[abstract]]Objective To present prenatal diagnosis and molecular genetic analyses of mosaic trisomy...
Objective To present prenatal diagnosis and molecular genetic analyses of mosaic trisomy 7 Materials...
Mosaic trisomy 13 is estimated to occur in 5% of all trisomy 13 cases. Presentation of trisomy 13 mo...