(Q43449045)

23 November 2017

Prenatal findings in children with early postnatal diagnosis of CHARGE syndrome (English)

1 reference

23 November 2017

5

1 reference

Brigitte Gilbert-Dussardier

23 November 2017

8

object named as

Brigitte Gilbert-Dussardier

1 reference

23 November 2017

Tiffany Busa

1

1 reference

23 November 2017

Marine Legendre

2

1 reference

23 November 2017

Marie Bauge

3

1 reference

23 November 2017

Edwin Quarello

4

1 reference

23 November 2017

Frederic Bilan

6

1 reference

23 November 2017

Sabine Sigaudy

7

1 reference

23 November 2017

Nicole Philip

9

1 reference

23 November 2017

9 April 2016

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23 November 2017

1 reference

23 November 2017

36

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23 November 2017

6

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23 November 2017

561-567

1 reference

Choanal atresia and associated multiple anomalies

23 November 2017

1 reference

Coloboma, congenital heart disease, and choanal atresia with multiple anomalies: CHARGE association

21 January 2018

1 reference

An epidemiological analysis of CHARGE syndrome: preliminary results from a Canadian study

21 January 2018

1 reference

Mutation update on the CHD7 gene involved in CHARGE syndrome

21 January 2018

1 reference

CHARGE association: an update and review for the primary pediatrician

21 January 2018

1 reference

Mutations in a new member of the chromodomain gene family cause CHARGE syndrome

21 January 2018

1 reference

CHD7 mutations and CHARGE syndrome: the clinical implications of an expanding phenotype.

21 January 2018

1 reference

CHARGE syndrome: the phenotypic spectrum of mutations in the CHD7 gene

21 January 2018

1 reference

CHARGE Syndrome-a five case study of the syndrome characteristics and health care consumption during the first year in life.

21 January 2018

1 reference

Antenatal spectrum of CHARGE syndrome in 40 fetuses with CHD7 mutations.

21 January 2018

1 reference

Atypical phenotypes associated with pathogenic CHD7 variants and a proposal for broadening CHARGE syndrome clinical diagnostic criteria.

21 January 2018

1 reference

The cardiac phenotype in patients with a CHD7 mutation.

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1002/PD.4825

1 reference

23 November 2017

1 reference