𝔖 Bobbio Scriptorium
✦   LIBER   ✦

The origin of aneuploidy: Bivalent instability and the maternal age effect in trisomy 21 Down syndrome

✍ Scribed by Hultén, M. A.


Publisher
John Wiley and Sons
Year
2005
Tongue
English
Weight
255 KB
Volume
37
Category
Article
ISSN
0148-7299

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


Effect of maternal age curve on the pred
✍ H. S. Cuckle 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 125 KB 👁 2 views

The effect of the choice of maternal age-specific prevalence curve on the model predicted Down syndrome detection rate was examined. All 19 published regression curves from 11 birth prevalence series in four meta-analyses were included. The detection rate for a five per cent false-positive rate was

The effect of differences in the distrib
✍ T. Huang; H. C. Watt; N. J. Wald 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 226 KB 👁 2 views

We aimed to determine how differences in the age at which women had their pregnancies influenced the expected detection and false-positive rates of serum screening for Down 's syndrome (i) between 1970 and 1993 in England and Wales, and (ii) between regions and districts of England and Wales in 1991

Maternal age-specific risk of Down syndr
✍ Bor-Ching Sheu; Ming-Kwang Shyu; Chien-Nan Lee; Bo-Jein Kuo; Yun-Ying Tseng; Fon 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 185 KB 👁 1 views

This study is a novel approach in establishing the maternal age-specific risk for Down syndrome screening in an Asian population. The relative frequency by one-year maternal age interval in women who had live births in the Taiwan area between 1975 and 1995 was used as the age-specific distribution o

The phenotype of persons having mosaicis
✍ Paulie Papavassiliou; Timothy P. York; Nurcan Gursoy; Gloria Hill; Lauren Vanner 📂 Article 📅 2009 🏛 John Wiley and Sons 🌐 English ⚖ 408 KB 👁 1 views

## Abstract Little is known about the pathogenesis of the phenotype in individuals with trisomy 21 mosaicism and Down syndrome. The primary goal of this study was to identify factors contributing to the observed phenotypic variation by evaluating 107 individuals having trisomy 21 mosaicism. To inve