(Q33681429)

28 July 2017

title

Further evidence for the involvement of human chromosome 6p24 in the aetiology of orofacial clefting (English)

1 reference

28 July 2017

Davies AF

1

1 reference

28 July 2017

Imaizumi K

2

1 reference

28 July 2017

Mirza G

3

1 reference

28 July 2017

Stephens RS

4

1 reference

28 July 2017

Kuroki Y

5

1 reference

28 July 2017

Matsuno M

6

1 reference

28 July 2017

Ragoussis J

7

1 reference

28 July 2017

language of work or name

English

0 references

publication date

1 October 1998

1 reference

Journal of Medical Genetics

28 July 2017

published in

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28 July 2017

volume

35

1 reference

28 July 2017

issue

10

1 reference

28 July 2017

page(s)

857-861

1 reference

Associated malformations in infants with cleft lip and palate: a prospective, population-based study.

28 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051465

An integrated map of human chromosome 6p23.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051465

Transcription factor AP-2 essential for cranial closure and craniofacial development

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051465

Eleven new cases of del(9p) and features from 80 cases

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051465

Partial deletion of chromosome 6p: delineation of the syndrome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051465

A detailed investigation of two cases exhibiting characteristics of the 6p deletion syndrome.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051465

Association of autosomal dominant cleft lip and palate and translocation 6p23;9q22.3

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051465

Whom would you trust with your genetic information?

30 October 2018

1 reference

12 December 2020

Suggestion of linkage of a major locus for nonsyndromic orofacial cleft with F13A and tentative assignment to chromosome 6

1 reference

12 December 2020

Evidence of a locus for orofacial clefting on human chromosome 6p24 and STS content map of the region

1 reference

12 December 2020

Construction and analysis of a sequence-ready map in 4q25: Rieger syndrome can be caused by haploinsufficiency of RIEG, but also by chromosome breaks approximately 90 kb upstream of this gene

1 reference

12 December 2020

Identifiers

DOI

10.1136/JMG.35.10.857

1 reference

28 July 2017

1 reference

28 July 2017

1 reference