Partial trisomy of the long arm of chromosome 1: Prenatal diagnosis, clinical evaluation and cytogenetic findings. Case report and review of the literature

Author:

Cambosu Francesca,Capobianco Giampiero,Fogu Giuseppina,Bandiera Pasquale,Pirino Alessio,Moro Maria Antonietta,Sanna Raimonda,Soro Giovanna,Dessole Margherita,Montella Andrea

Publisher

Wiley

Subject

Obstetrics and Gynaecology

Reference22 articles.

1. Direct prenatal chromosome diagnosis of a malignancy;Hecht;Cancer Genet Cytogenet,1984

2. Double autosomal trisomy (1q21.2----qter and 14pter----q13) in a female fetus with nuchal oedema;Fryns;Ann Genet,1987

3. Monozygotic twins discordant for partial trisomy 1;Watson;Obstet Gynecol,1990

4. An unusual mosaic karyotype detected through prenatal diagnosis with duplication of 1q and 19p and associated teratoma development;Schwartz;Teratology,1992

5. Prenatal diagnosis of partial trisomy 1q using fluorescent in situ hybridization;DuPont;Am J Med Genet,1994

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