๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Persistence of a monosomic cell line in a fetus with mosaic trisomy 8

โœ Scribed by Daniela Turchetti; Eva Pompilii; Elisabetta Magrini; Maria Paola Bonasoni; Maria Carla Pittalis; Maria Segata; Annalisa Pession; Donatella Santini; Gianluigi Pilu; Marco Seri


Publisher
John Wiley and Sons
Year
2011
Tongue
English
Weight
192 KB
Volume
155
Category
Article
ISSN
1552-4825

No coin nor oath required. For personal study only.


๐Ÿ“œ SIMILAR VOLUMES


Ectopia cordis in a fetus with mosaic tr
โœ Christos Arnaoutoglou; Soultana Meditskou; Anastasia Keivanidou; Marilena Mantho ๐Ÿ“‚ Article ๐Ÿ“… 2010 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 288 KB

## Abstract Ectopia cordis and mosaic trisomy 16 are two rare fetal anomalies, which have not been reported in association. We report a case of an isolated ectopia cordis at 11^+3^ weeks. Subsequent embryological examination confirmed thoracic ectopia cordis with normal heart structure and array co

Trisomy 8 mosaicism in a with patient te
โœ G๏ฟฝtze, Annemarie; Krebs, Petra; Stumm, Markus; Wieacker, Peter; Allhoff, Ernst P ๐Ÿ“‚ Article ๐Ÿ“… 1999 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 8 KB ๐Ÿ‘ 2 views

## Trisomy 8 Mosaicism in a Patient With Tetraamelia To the Editor: Trisomy 8 is detected in 0.8% of spontaneous abortions . In neoplasias, especially in myeloid leukaemias, trisomy 8 is a frequent somatic aberration . In liveborn infants trisomy 8 almost always is a mosaic condition. The frequen

Trisomy 8 mosaicism in a patient with he
โœ Fowzan S. Alkuraya; David J. Harris ๐Ÿ“‚ Article ๐Ÿ“… 2005 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 112 KB ๐Ÿ‘ 1 views

Constitutional trisomy 8 mosaicism (CT8M) is a relatively rare trisomy in humans with a characteristic phenotype. We report an infant with the characteristic CT8M phenotype in addition to heterotaxia. A number of chromosomal abnormalities have been reported in association with laterality defects but

TRISOMY 2: CONFINED PLACENTAL MOSAICISM
โœ ILANA ARIEL; ISRAELA LERER; SIMCHA YAGEL; RACHEL COHEN; ZIVA BEN-NERIAH; DVORAH ๐Ÿ“‚ Article ๐Ÿ“… 1997 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 272 KB ๐Ÿ‘ 2 views

In a pregnancy that was monitored due to increased risk for Down syndrome in the triple test, a normal karyotype was found in amniocentesis. Follow-up by serial ultrasound examinations revealed intrauterine growth retardation (IUGR) at 20 weeks of gestation. The parents decided to terminate the preg