Risk of Mosaicism and Uniparental Disomy Associated with the Prenatal Diagnosis of a Non-Homologous Robertsonian Translocation Carrier

Publisher： Karger

E-ISSN： 1421-9964|19|5|399-403

ISSN： 1015-3837

Source： Fetal Diagnosis and Therapy, Vol.19, Iss.5, 2004-08, pp. : 399-403

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content

Prenatal Diagnosis of Trisomy 2 Mosaicism: A Case Report

By  

Fetal Diagnosis and Therapy, Vol. 19, Iss. 6, 2004-11 ,pp. : 488-490

Karger

Access to resources Recommend Favorite

Two Unusual Cases of Haemoglobin Bart's Hydrops Fetalis due to Uniparental Disomy or Non-Paternity

By  

Fetal Diagnosis and Therapy, Vol. 35, Iss. 4, 2013-09 ,pp. : 306-308

Karger

Access to resources Recommend Favorite

Unexpected Inherited Chromosomal Translocation during Prenatal Diagnosis for Maternal Age: Risk for a Nondetectable Karyotype Imbalance in Offspring

By  

Fetal Diagnosis and Therapy, Vol. 13, Iss. 5, 1998-11 ,pp. : 271-275

Karger

Access to resources Recommend Favorite

Recurrent Trisomy 21 and Uniparental Disomy 21 in a Family

By  

Fetal Diagnosis and Therapy, Vol. 18, Iss. 6, 2003-10 ,pp. : 454-458

Karger

Access to resources Recommend Favorite

Prenatal Diagnosis of 18q-Syndrome: A Case of Fetal Mosaicism with a Normal Karyotype in Chorionic Villi

By  

Fetal Diagnosis and Therapy, Vol. 28, Iss. 3, 2010-09 ,pp. : 180-185

Karger

Access to resources Recommend Favorite