(Q33597626)

28 July 2017

Miller syndrome (postaxial acrofacial dysostosis): further evidence for autosomal recessive inheritance and expansion of the phenotype (English)

1 reference

28 July 2017

1 reference

Ogilvy-Stuart AL

1

1 reference

PubMed ID

1941965

28 July 2017

Parsons AC

series ordinal

2

1 reference

PubMed ID

1941965

28 July 2017

language of work or name

English

0 references

publication date

1 October 1991

1 reference

Journal of Medical Genetics

28 July 2017

1 reference

28 July 2017

28

1 reference

28 July 2017

695-700

1 reference

28 July 2017

10

1 reference

Miller's syndrome. Anaesthetic management of postaxial acrofacial dysostosis.

28 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017057

Postaxial acrofacial dysostosis (Miller) 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=1017057

Acrofacial dysostosis with postaxial limb deficiency

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017057

Postaxial acrofacial dysostosis syndrome with microcephaly, seizures and profound mental retardation

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017057

Fibular a/hypoplasia: review and documentation of the fibular developmental field

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017057

Postaxial acrofacial dysostosis or Miller syndrome. A case report

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017057

Postaxial acrofacial dysostosis 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=1017057

Robin sequence and oligodactyly in mother and son

21 June 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/1941965

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Phenotype variability in the Miller acrofacial dysostosis syndrome. Report of two further patients

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/1941965

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Robin sequence and oligodactyly in mother and son--probably a further example of the postaxial acrofacial dysostosis syndrome

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/1941965

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1136/JMG.28.10.695

1 reference

28 July 2017

1 reference

28 July 2017

1 reference

PubMed ID

1941965