Recurrence risk figures for isolated tetralogy of Fallot after screening for 22q11 microdeletion (Q33678515)

28 July 2017

title

Recurrence risk figures for isolated tetralogy of Fallot after screening for 22q11 microdeletion (English)

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28 July 2017

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Digilio MC

1

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28 July 2017

Marino B

2

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28 July 2017

Giannotti A

3

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28 July 2017

Toscano A

4

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28 July 2017

Dallapiccola B

5

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28 July 2017

language of work or name

English

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publication date

1 March 1997

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Journal of Medical Genetics

28 July 2017

published in

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28 July 2017

volume

34

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28 July 2017

issue

3

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28 July 2017

page(s)

188-190

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Comparison of occurrence of genetic syndromes in ventricular septal defect with pulmonic stenosis (classic tetralogy of Fallot) versus ventricular septal defect with pulmonic atresia.

28 July 2017

cites work

1 reference

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Associated cardiac anomalies in isolated and syndromic patients with tetralogy of Fallot.

21 June 2018

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A single major-gene defect underlying cardiac conotruncal malformations interferes with myocardial growth during embryonic development: studies in the CTD line of keeshond dogs

21 June 2018

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Microdeletions of chromosomal region 22q11 in patients with congenital conotruncal cardiac defects

21 June 2018

1 reference

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A family study of Fallot's tetralogy

21 June 2018

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Multifactorial inheritance hypothesis for the etiology of congenital heart diseases. The genetic-environmental interaction

21 June 2018

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The developmental field concept.

21 June 2018

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Maternal transmission of congenital heart diseases: new recurrence risk figures and the questions of cytoplasmic inheritance and vulnerability to teratogens

21 June 2018

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Cardiovascular anomalies in DiGeorge syndrome and importance of neural crest as a possible pathogenetic factor.

21 June 2018

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Cardiac and noncardiac malformations: observations in a population-based study

21 June 2018

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Familial risks of congenital heart defect assessed in a population-based epidemiologic study.

21 June 2018

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The inheritance of conotruncal malformations: a review and report of two siblings with tetralogy of Fallot with pulmonary atresia

21 June 2018

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Tetralogy of Fallot in three siblings: a familial study and review of the literature.

21 June 2018

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The recurrence risk in congenital heart disease

21 June 2018

1 reference

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Conotruncal malformation complex: examples of possible monogenic inheritance

21 June 2018

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The evolution of specific genetic and environmental counseling in congenital heart diseases

21 June 2018

1 reference

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Maternal periconceptional use of multivitamins and reduced risk for conotruncal heart defects and limb deficiencies among offspring.

21 June 2018

1 reference

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Tetralogy of Fallot in three sibs

30 October 2018

1 reference

12 December 2020

Deletions within chromosome 22q11 in familial congenital heart disease

1 reference

12 December 2020

22q11 deletions in isolated and syndromic patients with tetralogy of Fallot

1 reference

12 December 2020

Familial non-syndromic conotruncal defects are not associated with a 22q11 microdeletion

1 reference

12 December 2020

Cardiac malformations in the velocardiofacial syndrome

1 reference

12 December 2020

Congenital cardiac anomalies associated with the DiGeorge syndrome: a neonatal experience

1 reference

12 December 2020

Identifiers

DOI

10.1136/JMG.34.3.188

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28 July 2017

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28 July 2017

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