(Q35446830)

8 August 2017

title

An aetiological classification of birth defects for epidemiological research (English)

1 reference

8 August 2017

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D Wellesley

1

1 reference

8 August 2017

P Boyd

series ordinal

2

1 reference

8 August 2017

H Dolk

series ordinal

3

1 reference

8 August 2017

S Pattenden

series ordinal

4

1 reference

8 August 2017

language of work or name

English

0 references

publication date

1 January 2005

1 reference

Journal of Medical Genetics

8 August 2017

published in

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8 August 2017

volume

42

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8 August 2017

issue

1

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8 August 2017

page(s)

54-57

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Evidence for selective advantage of pathogenic FGFR2 mutations in the male germ line

8 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735901

Rare congenital disorders, imprinted genes, and assisted reproductive technology

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735901

Association of in vitro fertilization with Beckwith-Wiedemann syndrome and epigenetic alterations of LIT1 and H19

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735901

Intracytoplasmic sperm injection may increase the risk of imprinting defects

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735901

Exclusive paternal origin of new mutations in Apert syndrome

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735901

A developmental approach to the classification of birth defects.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735901

Spontaneous mutation and parental age in humans

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735901

On the parental origin of de novo mutation in man.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735901

Guidelines for case classification for the National Birth Defects Prevention Study

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735901

A paternal wash in Apert syndrome

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735901

Population surveillance of sentinel anomalies

26 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/15635076

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1136/JMG.2004.023309

1 reference

8 August 2017

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8 August 2017

1 reference