(Q83121118)

English

MTHFR 677 TT genotype in a mother and her child with Down syndrome, atrioventricular canal and exstrophy of the bladder: implications of a mutual genetic risk factor?

scientific article published on 07 April 2006

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scholarly article

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16602006%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

MTHFR 677 TT genotype in a mother and her child with Down syndrome, atrioventricular canal and exstrophy of the bladder: implications of a mutual genetic risk factor? (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16602006%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

1 reference

based on heuristic

inferred from title

1

object named as

Heiko Reutter

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16602006%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

author name string

Regina C Betz

2

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16602006%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

Michael Ludwig

3

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16602006%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

Thomas M Boemers

4

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16602006%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

publication date

7 April 2006

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16602006%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

European Journal of Pediatrics

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16602006%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

165

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16602006%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

8

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Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16602006%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

566-568

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16602006%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

Folate-related genes and omphalocele

1 reference

https://pubmed.ncbi.nlm.nih.gov/16602006

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Is there an association of Down Syndrome and omphalocele?

1 reference

https://pubmed.ncbi.nlm.nih.gov/16602006

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Polymorphisms in genes involved in folate metabolism as maternal risk factors for Down syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/16602006

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase

1 reference

https://pubmed.ncbi.nlm.nih.gov/16602006

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Maternal methylenetetrahydrofolate reductase deficiency and low dietary folate lead to adverse reproductive outcomes and congenital heart defects in mice.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16602006

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Occurrence of omphalocele in relation to maternal multivitamin use: a population-based study

1 reference

https://pubmed.ncbi.nlm.nih.gov/16602006

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

MTRR and MTHFR polymorphism: link to Down syndrome?

1 reference

https://pubmed.ncbi.nlm.nih.gov/16602006

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Genetic and molecular biological aspects of the bladder exstrophy-epispadias complex (BEEC)]

1 reference

https://pubmed.ncbi.nlm.nih.gov/16602006

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Abnormal folate metabolism and genetic polymorphism of the folate pathway in a child with Down syndrome and neural tube defect.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16602006

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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