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

Publisher： Karger

E-ISSN： 1421-9964|28|3|180-185

ISSN： 1015-3837

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

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

A Comparison of in vitro Culture of Fetal Nucleated Erythroblasts from Fetal Chorionic Villi and Maternal Peripheral Blood for Noninvasive Prenatal Diagnosis

By  

Fetal Diagnosis and Therapy, Vol. 32, Iss. 3, 2012-06 ,pp. : 194-200

Karger

Access to resources Recommend Favorite

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

Prenatal Diagnosis of an Epignathus Associated with a 49,XXXXY Karyotype – A Case Report

By  

Fetal Diagnosis and Therapy, Vol. 24, Iss. 3, 2008-10 ,pp. : 313-317

Karger

Access to resources Recommend Favorite

Elevated Interferon-Alpha in Fetal Blood in the Prenatal Diagnosis of Aicardi-Goutières Syndrome

By  

Fetal Diagnosis and Therapy, Vol. 21, Iss. 1, 2005-12 ,pp. : 153-155

Karger

Access to resources Recommend Favorite

Too Late Prenatal Diagnosis of Fetal Toxoplasmosis: A Case Report

By  

Fetal Diagnosis and Therapy, Vol. 20, Iss. 3, 2005-04 ,pp. : 190-193

Karger

Access to resources Recommend Favorite