Nuchal translucency thickness in the prediction of unbalanced translocations

Author:

Arigita Marta1,Grande Maribel2,Mula Raquel2,Borobio Virginia2,Sanchez Aurora3,Soler Anna3,Borrell Antoni2

Affiliation:

1. Department of Obstetrics and Gynecology; Hospital General de l'Hospitalet; L'Hospitalet del Llobregat Barcelona Catalonia Spain

2. Prenatal Diagnosis Unit, Department of Maternal-Fetal Medicine, ICGON; Hospital Clinic Barcelona, University of Barcelona; Barcelona Catalonia Spain

3. Biomedical Diagnosis Center; Hospital Clinic Barcelona; Barcelona Catalonia Spain

Publisher

Wiley

Subject

Genetics (clinical),Obstetrics and Gynecology

Reference22 articles.

1. The frequency and mutation rate of balanced autosomal rearrangements in man estimated from prenatal genetic studies for advanced maternal age;Van Dyke;Am J Hum Genet,1983

2. Detection of balanced chromosomal rearrangements in 445 couples with repeated abortion and cytogenetic prenatal testing in carriers;Fortuny;Fertil Steril,1988

3. Patterns of chromosomal translocations identified by a birth defects registry, Hawaii, 1986-2000;Forrester;Genet Test,2004

4. Fetal nuchal translucency: ultrasound screening for chromosomal defects in first trimester of pregnancy;Nicolaides;BMJ,1992

5. Increased nuchal translucency and normal karyotype: perinatal and pediatric outcomes at 2 years of age;Mula;Ultrasound Obstet Gynecol,2012

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