(Q81338465)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15679998%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

title

New trends in chromosomal investigation in children with cardiovascular malformations (English)

1 reference

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7 January 2020

author name string

Ruth Schellberg

1

1 reference

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7 January 2020

Gesa Schwanitz

2

1 reference

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7 January 2020

Lutz Grävinghoff

3

1 reference

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7 January 2020

Rolf Kallenberg

4

1 reference

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7 January 2020

Detlef Trost

5

1 reference

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7 January 2020

Ruth Raff

6

1 reference

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7 January 2020

Walter Wiebe

7

1 reference

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7 January 2020

publication date

1 December 2004

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15679998%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

published in

Cardiology in the Young

1 reference

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7 January 2020

volume

14

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7 January 2020

issue

6

1 reference

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7 January 2020

page(s)

622-629

1 reference

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Telomeres: a diagnosis at the end of the chromosomes

7 January 2020

cites work

1 reference

https://api.crossref.org/works/10.1017%2FS1047951104006079

7 January 2021

Associations between chromosomal anomalies and congenital heart defects: a database search.

1 reference

https://api.crossref.org/works/10.1017%2FS1047951104006079

7 January 2021

Congenital cardiovascular malformations associated with chromosome abnormalities: an epidemiologic study

1 reference

https://api.crossref.org/works/10.1017%2FS1047951104006079

7 January 2021

High level of unequal meiotic crossovers at the origin of the 22q11. 2 and 7q11.23 deletions.

1 reference

https://api.crossref.org/works/10.1017%2FS1047951104006079

7 January 2021

Mutational mechanisms of Williams-Beuren syndrome deletions

1 reference

https://api.crossref.org/works/10.1017%2FS1047951104006079

7 January 2021

Advances in molecular cytogenetics for the evaluation of mental retardation

1 reference

https://api.crossref.org/works/10.1017%2FS1047951104006079

7 January 2021

22q11.2 deletions in a series of patients with non-selective congenital heart defects: incidence, type of defects and parental origin

1 reference

https://api.crossref.org/works/10.1017%2FS1047951104006079

7 January 2021

Investigation of meiotic rearrangements in DGS/VCFS patients with a microdeletion 22q11.2.

1 reference

https://api.crossref.org/works/10.1017%2FS1047951104006079

7 January 2021

Microdeletion 22q11 in complex cardiovascular malformations

1 reference

https://api.crossref.org/works/10.1017%2FS1047951104006079

7 January 2021

Congenital heart disease in a cohort of 19,502 births with long-term follow-up

1 reference

https://api.crossref.org/works/10.1017%2FS1047951104006079

7 January 2021

Frequency of a 22q11 deletion in patients with conotruncal cardiac malformations: a prospective study

1 reference

https://api.crossref.org/works/10.1017%2FS1047951104006079

7 January 2021

Subtle chromosomal rearrangements in children with unexplained mental retardation

1 reference

https://api.crossref.org/works/10.1017%2FS1047951104006079

7 January 2021

The highest gene concentrations in the human genome are in telomeric bands of metaphase chromosomes

1 reference

https://api.crossref.org/works/10.1017%2FS1047951104006079

7 January 2021

10.1017/S1047951104006079

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15679998%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

1 reference