A familial congenital heart disease with a possible multigenic origin involving a mutation in BMPR1A

to related objects

Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 2045-2322

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: A familial congenital heart disease with a possible multigenic origin involving a mutation in BMPR1A ; volume:9 ; number:1 ; day:27 ; month:2 ; year:2019 ; pages:1-12 ; date:12.2019
Scientific reports ; 9, Heft 1 (27.2.2019), 1-12, 12.2019

Classification: Naturwissenschaften

Creator: Demal, Till Joscha
Heise, Melina
Reiz, Benedikt
Dogra, Deepika
Brænne, Ingrid
Reichenspurner, Hermann
Männer, Jörg
Aherrahrou, Zouhair
Schunkert, Heribert
Erdmann, Jeanette
Seyfried, Salim

Contributor: SpringerLink (Online service)

DOI: 10.1038/s41598-019-39648-7

URN: urn:nbn:de:101:1-2019031721145964131224

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

Last update: 14.08.2025, 10:57 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

Demal, Till Joscha
Heise, Melina
Reiz, Benedikt
Dogra, Deepika
Brænne, Ingrid
Reichenspurner, Hermann
Männer, Jörg
Aherrahrou, Zouhair
Schunkert, Heribert
Erdmann, Jeanette
Seyfried, Salim
SpringerLink (Online service)

Other Objects (12)

Longitudinal familial analysis of blood pressure involving parametric (co)variance functions

Possible New Strategies for the Treatment of Congenital Hyperinsulinism

Extreme intra-familial variability of congenital central hypoventilation syndrome: a case series

Origin of copper dissolution under electrocatalytic reduction conditions involving amines

Angiogenic biomarkers in children with congenital heart disease: possible implications

Congenital Anatomical Variant with Cranial Origin of Internal Iliac Arteries

The mutation spectrum in familial versus sporadic congenital cataract based on next-generation sequencing

Variation in WNT7A is unlikely to be a cause of familial Congenital Talipes Equinovarus

Breyite inclusions in diamond: experimental evidence for possible dual origin

A possible relationship between respiratory muscle weakness and familial mediterranean fever: a case report

Familial tetrasomy 4q35.2 associated with congenital diaphragmatic hernia and unilateral renal agenesis: a case report

Congenital hypopituitarism and multiple midline defects in a newborn with non-familial Cat Eye syndrome

Longitudinal familial analysis of blood pressure involving parametric (co)variance functions

Possible New Strategies for the Treatment of Congenital Hyperinsulinism

Extreme intra-familial variability of congenital central hypoventilation syndrome: a case series

Origin of copper dissolution under electrocatalytic reduction conditions involving amines

Angiogenic biomarkers in children with congenital heart disease: possible implications

Congenital Anatomical Variant with Cranial Origin of Internal Iliac Arteries

The mutation spectrum in familial versus sporadic congenital cataract based on next-generation sequencing

Variation in WNT7A is unlikely to be a cause of familial Congenital Talipes Equinovarus

Breyite inclusions in diamond: experimental evidence for possible dual origin

A possible relationship between respiratory muscle weakness and familial mediterranean fever: a case report

Familial tetrasomy 4q35.2 associated with congenital diaphragmatic hernia and unilateral renal agenesis: a case report

Congenital hypopituitarism and multiple midline defects in a newborn with non-familial Cat Eye syndrome

Longitudinal familial analysis of blood pressure involving parametric (co)variance functions

Possible New Strategies for the Treatment of Congenital Hyperinsulinism

Extreme intra-familial variability of congenital central hypoventilation syndrome: a case series

Origin of copper dissolution under electrocatalytic reduction conditions involving amines

Angiogenic biomarkers in children with congenital heart disease: possible implications

Congenital Anatomical Variant with Cranial Origin of Internal Iliac Arteries

The mutation spectrum in familial versus sporadic congenital cataract based on next-generation sequencing

Variation in WNT7A is unlikely to be a cause of familial Congenital Talipes Equinovarus

Breyite inclusions in diamond: experimental evidence for possible dual origin

A possible relationship between respiratory muscle weakness and familial mediterranean fever: a case report

Familial tetrasomy 4q35.2 associated with congenital diaphragmatic hernia and unilateral renal agenesis: a case report

Congenital hypopituitarism and multiple midline defects in a newborn with non-familial Cat Eye syndrome

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.

A familial congenital heart disease with a possible multigenic origin involving a mutation in BMPR1A

Object Details

References and Relationships

Classification and Topics

Contributors, Places and Time

Further information

Data provider

Associated

Other Objects (12)

Longitudinal familial analysis of blood pressure involving parametric (co)variance functions

Possible New Strategies for the Treatment of Congenital Hyperinsulinism

Extreme intra-familial variability of congenital central hypoventilation syndrome: a case series

Origin of copper dissolution under electrocatalytic reduction conditions involving amines

Angiogenic biomarkers in children with congenital heart disease: possible implications

Congenital Anatomical Variant with Cranial Origin of Internal Iliac Arteries

The mutation spectrum in familial versus sporadic congenital cataract based on next-generation sequencing

Variation in WNT7A is unlikely to be a cause of familial Congenital Talipes Equinovarus

Breyite inclusions in diamond: experimental evidence for possible dual origin

A possible relationship between respiratory muscle weakness and familial mediterranean fever: a case report

Familial tetrasomy 4q35.2 associated with congenital diaphragmatic hernia and unilateral renal agenesis: a case report

Congenital hypopituitarism and multiple midline defects in a newborn with non-familial Cat Eye syndrome

Longitudinal familial analysis of blood pressure involving parametric (co)variance functions

Possible New Strategies for the Treatment of Congenital Hyperinsulinism

Extreme intra-familial variability of congenital central hypoventilation syndrome: a case series

Origin of copper dissolution under electrocatalytic reduction conditions involving amines

Angiogenic biomarkers in children with congenital heart disease: possible implications

Congenital Anatomical Variant with Cranial Origin of Internal Iliac Arteries

The mutation spectrum in familial versus sporadic congenital cataract based on next-generation sequencing

Variation in WNT7A is unlikely to be a cause of familial Congenital Talipes Equinovarus

Breyite inclusions in diamond: experimental evidence for possible dual origin

A possible relationship between respiratory muscle weakness and familial mediterranean fever: a case report

Familial tetrasomy 4q35.2 associated with congenital diaphragmatic hernia and unilateral renal agenesis: a case report

Congenital hypopituitarism and multiple midline defects in a newborn with non-familial Cat Eye syndrome

Longitudinal familial analysis of blood pressure involving parametric (co)variance functions

Possible New Strategies for the Treatment of Congenital Hyperinsulinism

Extreme intra-familial variability of congenital central hypoventilation syndrome: a case series

Origin of copper dissolution under electrocatalytic reduction conditions involving amines

Angiogenic biomarkers in children with congenital heart disease: possible implications

Congenital Anatomical Variant with Cranial Origin of Internal Iliac Arteries

The mutation spectrum in familial versus sporadic congenital cataract based on next-generation sequencing

Variation in WNT7A is unlikely to be a cause of familial Congenital Talipes Equinovarus

Breyite inclusions in diamond: experimental evidence for possible dual origin

A possible relationship between respiratory muscle weakness and familial mediterranean fever: a case report

Familial tetrasomy 4q35.2 associated with congenital diaphragmatic hernia and unilateral renal agenesis: a case report

Congenital hypopituitarism and multiple midline defects in a newborn with non-familial Cat Eye syndrome

Related objects

Reset password