Prenatal MRI Diagnosis of Hirschsprung's Disease at 29 Weeks' Gestational Age in a Fetus with Heterotaxy and Polysplenia Syndrome

Publisher： Karger

E-ISSN： 1421-9964|40|3|235-240

ISSN： 1015-3837

Source： Fetal Diagnosis and Therapy, Vol.40, Iss.3, 2015-02, pp. : 235-240

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 Nonmosaic Trisomy 9 in a Fetus with Severe Renal Disease

By  

Gynecologic and Obstetric Investigation, Vol. 48, Iss. 1, 1999-07 ,pp. : 69-72

Karger

Access to resources Recommend Favorite

Prenatal Diagnosis of a Fetus Affected with Down Syndrome and Deletion 1p36 Syndrome by Fluorescence in situ Hybridization and Spectral Karyotyping

By  

Fetal Diagnosis and Therapy, Vol. 19, Iss. 4, 2004-06 ,pp. : 356-360

Karger

Access to resources Recommend Favorite

Ultrasonographic Diagnosis of Jarcho-Levin Syndrome at 20 Weeks’ Gestation in a Fetus without Previous Family History

By  

Fetal Diagnosis and Therapy, Vol. 20, Iss. 2, 2005-02 ,pp. : 136-140

Karger

Access to resources Recommend Favorite

Prenatal Diagnosis of Diastematomyelia in a 15-Week-Old Fetus

By  

Fetal Diagnosis and Therapy, Vol. 20, Iss. 4, 2005-06 ,pp. : 258-261

Karger

Access to resources Recommend Favorite

Prenatal Diagnosis of Urinary Ascites in a Fetus with Meningomyelocele

By  

Fetal Diagnosis and Therapy, Vol. 28, Iss. 1, 2010-04 ,pp. : 61-64

Karger

Access to resources Recommend Favorite