Prenatal ultrasound in fetuses with polycystic kidney appearance — expanding the diagnostic algorithm

to related objects

Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 1432-0711

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: Prenatal ultrasound in fetuses with polycystic kidney appearance — expanding the diagnostic algorithm ; day:31 ; month:10 ; year:2022 ; pages:1-14
Archives of gynecology and obstetrics ; (31.10.2022), 1-14

Creator: Simonini, Corinna
Fröschen, Eva-Maria
Nadal, Jennifer
Strizek, Brigitte
Berg, Christoph
Geipel, Annegret
Gembruch, Ulrich

Contributor: SpringerLink (Online service)

DOI: 10.1007/s00404-022-06814-8

URN: urn:nbn:de:101:1-2023011509033819697106

Rights: Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 15.08.2025, 7:30 AM CEST

Data provider

This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.

Show original at data provider

Associated

Simonini, Corinna
Fröschen, Eva-Maria
Nadal, Jennifer
Strizek, Brigitte
Berg, Christoph
Geipel, Annegret
Gembruch, Ulrich
SpringerLink (Online service)

Other Objects (12)

Prenatal phenotypes and pregnancy outcomes of fetuses with 16p11.2 microdeletion/microduplication

Prenatal Diagnosis and Outcome of Fetuses with Double-Inlet Left Ventricle

Two fetuses in one family of arterial tortuosity syndrome: prenatal ultrasound diagnosis

Prenatal diagnosis and early childhood outcome of fetuses with extremely large nuchal translucency

Chromosomal microarray analysis versus noninvasive prenatal testing in fetuses with increased nuchal translucency

Prenatal diagnosis, associated findings and postnatal outcome of fetuses with truncus arteriosus communis (TAC)

Prenatal diagnosis of 22q11.2 copy number abnormalities in fetuses via single nucleotide polymorphism array

Prenatal Diagnosis, Associated Findings, and Postnatal Outcome in Fetuses with Double Inlet Ventricle (DIV)

Prenatal diagnosis of 17q12 microdeletion and microduplication syndrome in fetuses with congenital renal abnormalities

A prenatal standard for fetal weight improves the prenatal diagnosis of small for gestational age fetuses in pregnancies at increased risk

Comparing levocardia and dextrocardia in fetuses with heterotaxy syndrome: prenatal features, clinical significance and outcomes

Prenatal phenotypes and pregnancy outcomes of fetuses with 16p11.2 microdeletion/microduplication

Prenatal Diagnosis and Outcome of Fetuses with Double-Inlet Left Ventricle

Two fetuses in one family of arterial tortuosity syndrome: prenatal ultrasound diagnosis

Prenatal diagnosis and early childhood outcome of fetuses with extremely large nuchal translucency

Chromosomal microarray analysis versus noninvasive prenatal testing in fetuses with increased nuchal translucency

Prenatal diagnosis, associated findings and postnatal outcome of fetuses with truncus arteriosus communis (TAC)

Prenatal diagnosis of 22q11.2 copy number abnormalities in fetuses via single nucleotide polymorphism array

Prenatal Diagnosis, Associated Findings, and Postnatal Outcome in Fetuses with Double Inlet Ventricle (DIV)

Prenatal diagnosis of 17q12 microdeletion and microduplication syndrome in fetuses with congenital renal abnormalities

A prenatal standard for fetal weight improves the prenatal diagnosis of small for gestational age fetuses in pregnancies at increased risk

Comparing levocardia and dextrocardia in fetuses with heterotaxy syndrome: prenatal features, clinical significance and outcomes

Prenatal phenotypes and pregnancy outcomes of fetuses with 16p11.2 microdeletion/microduplication

Prenatal Diagnosis and Outcome of Fetuses with Double-Inlet Left Ventricle

Two fetuses in one family of arterial tortuosity syndrome: prenatal ultrasound diagnosis

Prenatal diagnosis and early childhood outcome of fetuses with extremely large nuchal translucency

Chromosomal microarray analysis versus noninvasive prenatal testing in fetuses with increased nuchal translucency

Prenatal diagnosis, associated findings and postnatal outcome of fetuses with truncus arteriosus communis (TAC)

Prenatal diagnosis of 22q11.2 copy number abnormalities in fetuses via single nucleotide polymorphism array

Prenatal Diagnosis, Associated Findings, and Postnatal Outcome in Fetuses with Double Inlet Ventricle (DIV)

Prenatal diagnosis of 17q12 microdeletion and microduplication syndrome in fetuses with congenital renal abnormalities

A prenatal standard for fetal weight improves the prenatal diagnosis of small for gestational age fetuses in pregnancies at increased risk

Comparing levocardia and dextrocardia in fetuses with heterotaxy syndrome: prenatal features, clinical significance and outcomes

Cultural heritage institutions wishing to register will find more information here.

Fields marked * need to be filled in.

Username*

Please enter your username

Email*

Please enter your email address

Please do not fill this field

First name

Last name

Password*

Please enter your password

Confirm password*

Please enter the same password

I have read the terms of use and the privacy policy for the collection of personal data and accept them. *

This field is required.

I would like to subscribe to the newsletter of the Deutsche Digitale Bibliothek. See newsletter subscription info.

Account created

Your "My DDB" account has been successfully created. Before you can log in to your account, you must click the confirmation link in the message we just sent to the email address you provided.

Prenatal ultrasound in fetuses with polycystic kidney appearance — expanding the diagnostic algorithm

Object Details

References and Relationships

Contributors, Places and Time

Further information

Data provider

Associated

Other Objects (12)

Prenatal phenotypes and pregnancy outcomes of fetuses with 16p11.2 microdeletion/microduplication

Prenatal Diagnosis and Outcome of Fetuses with Double-Inlet Left Ventricle

Two fetuses in one family of arterial tortuosity syndrome: prenatal ultrasound diagnosis

Prenatal diagnosis and early childhood outcome of fetuses with extremely large nuchal translucency

Chromosomal microarray analysis versus noninvasive prenatal testing in fetuses with increased nuchal translucency

Prenatal diagnosis, associated findings and postnatal outcome of fetuses with truncus arteriosus communis (TAC)

Prenatal diagnosis, associated findings and postnatal outcome of fetuses with truncus arteriosus communis (TAC)

Prenatal diagnosis of 22q11.2 copy number abnormalities in fetuses via single nucleotide polymorphism array

Prenatal Diagnosis, Associated Findings, and Postnatal Outcome in Fetuses with Double Inlet Ventricle (DIV)

Prenatal diagnosis of 17q12 microdeletion and microduplication syndrome in fetuses with congenital renal abnormalities

A prenatal standard for fetal weight improves the prenatal diagnosis of small for gestational age fetuses in pregnancies at increased risk

Comparing levocardia and dextrocardia in fetuses with heterotaxy syndrome: prenatal features, clinical significance and outcomes

Prenatal phenotypes and pregnancy outcomes of fetuses with 16p11.2 microdeletion/microduplication

Prenatal Diagnosis and Outcome of Fetuses with Double-Inlet Left Ventricle

Two fetuses in one family of arterial tortuosity syndrome: prenatal ultrasound diagnosis

Prenatal diagnosis and early childhood outcome of fetuses with extremely large nuchal translucency

Chromosomal microarray analysis versus noninvasive prenatal testing in fetuses with increased nuchal translucency

Prenatal diagnosis, associated findings and postnatal outcome of fetuses with truncus arteriosus communis (TAC)

Prenatal diagnosis, associated findings and postnatal outcome of fetuses with truncus arteriosus communis (TAC)

Prenatal diagnosis of 22q11.2 copy number abnormalities in fetuses via single nucleotide polymorphism array

Prenatal Diagnosis, Associated Findings, and Postnatal Outcome in Fetuses with Double Inlet Ventricle (DIV)

Prenatal diagnosis of 17q12 microdeletion and microduplication syndrome in fetuses with congenital renal abnormalities

A prenatal standard for fetal weight improves the prenatal diagnosis of small for gestational age fetuses in pregnancies at increased risk

Comparing levocardia and dextrocardia in fetuses with heterotaxy syndrome: prenatal features, clinical significance and outcomes

Prenatal phenotypes and pregnancy outcomes of fetuses with 16p11.2 microdeletion/microduplication

Prenatal Diagnosis and Outcome of Fetuses with Double-Inlet Left Ventricle

Two fetuses in one family of arterial tortuosity syndrome: prenatal ultrasound diagnosis

Prenatal diagnosis and early childhood outcome of fetuses with extremely large nuchal translucency

Chromosomal microarray analysis versus noninvasive prenatal testing in fetuses with increased nuchal translucency

Prenatal diagnosis, associated findings and postnatal outcome of fetuses with truncus arteriosus communis (TAC)

Prenatal diagnosis, associated findings and postnatal outcome of fetuses with truncus arteriosus communis (TAC)

Prenatal diagnosis of 22q11.2 copy number abnormalities in fetuses via single nucleotide polymorphism array

Prenatal Diagnosis, Associated Findings, and Postnatal Outcome in Fetuses with Double Inlet Ventricle (DIV)

Prenatal diagnosis of 17q12 microdeletion and microduplication syndrome in fetuses with congenital renal abnormalities

A prenatal standard for fetal weight improves the prenatal diagnosis of small for gestational age fetuses in pregnancies at increased risk

Comparing levocardia and dextrocardia in fetuses with heterotaxy syndrome: prenatal features, clinical significance and outcomes

Related objects

Reset password