(Q58193256)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22391434%20AND%20SRC:MED&resulttype=core&format=json

25 January 2020

title

Association of DiGeorge anomaly and caudal dysplasia sequence in a neonate born to a diabetic mother (English)

1 reference

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25 January 2020

5

1 reference

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25 January 2020

Bruno Dallapiccola

8

1 reference

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25 January 2020

author name string

Silvia Placidi

2

1 reference

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25 January 2020

Paola Francalanci

3

1 reference

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25 January 2020

Rossella Capolino

4

1 reference

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25 January 2020

Bruno Marino

6

1 reference

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25 January 2020

Maria L Dentici

1

1 reference

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25 January 2020

Maria C Digilio

7

1 reference

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25 January 2020

publication date

6 March 2012

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22391434%20AND%20SRC:MED&resulttype=core&format=json

25 January 2020

published in

Cardiology in the Young

1 reference

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25 January 2020

volume

23

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25 January 2020

issue

1

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25 January 2020

page(s)

14-17

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Physical activity positively predicts bone architecture and bone strength in adolescent males and females

25 January 2020

cites work

1 reference

https://api.crossref.org/works/10.1017%2FS1047951112000194

Prevalence of the microdeletion 22q11 in newborn infants with congenital conotruncal cardiac anomalies

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1047951112000194

DiGeorge syndrome: an historical review of clinical and cytogenetic features

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1047951112000194

A new concept of the cellular basis of immunity

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1047951112000194

Infants of diabetic mothers are at increased risk for the oculo-auriculo-vertebral sequence: A case-based and case-control approach

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1047951112000194

Maternal diabetes: an independent risk factor for major cardiovascular malformations with increased mortality of affected infants

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1047951112000194

Epidemiological analysis of outcomes of pregnancy in diabetic mothers: identification of the most characteristic and most frequent congenital anomalies

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1047951112000194

The syndrome of caudal dysplasia: a review, including etiologic considerations and evidence of heterogeneity

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1047951112000194

Chromosome 22q11.2 microdeletion in children with conotruncal heart defects: frequency, associated cardiovascular anomalies, and outcome following cardiac surgery

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1047951112000194

Atrioventricular septal defect with pulmonary atresia in DiGeorge anomaly: expansion of the cardiac phenotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1047951112000194

7 January 2021

Maternal diabetes causing DiGeorge anomaly and renal agenesis

1 reference

https://api.crossref.org/works/10.1017%2FS1047951112000194

7 January 2021

DiGeorge anomaly with renal agenesis in infants of mothers with diabetes

1 reference

https://api.crossref.org/works/10.1017%2FS1047951112000194

7 January 2021

Epidemiological analysis of outcomes of pregnancy in gestational diabetic mothers

1 reference

https://api.crossref.org/works/10.1017%2FS1047951112000194

7 January 2021

Frequency of 22q11 deletions in patients with conotruncal defects

1 reference

https://api.crossref.org/works/10.1017%2FS1047951112000194

7 January 2021

Anatomic patterns of conotruncal defects associated with deletion 22q11

1 reference

https://api.crossref.org/works/10.1017%2FS1047951112000194

7 January 2021

Maternal diabetes and cardiovascular malformations: predominance of double outlet right ventricle and truncus arteriosus

1 reference

https://api.crossref.org/works/10.1017%2FS1047951112000194

7 January 2021

Variation in prevalence of chromosome 22q11 deletion in subtypes of conotruncal defect in 254 children.

1 reference

https://api.crossref.org/works/10.1017%2FS1047951112000194

7 January 2021

10.1017/S1047951112000194

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22391434%20AND%20SRC:MED&resulttype=core&format=json

25 January 2020

1 reference