(Q41671809)

6 October 2017

A new form of autosomal dominant arthrogryposis (English)

1 reference

6 October 2017

Lai MM

1

1 reference

6 October 2017

Tettenborn MA

2

1 reference

6 October 2017

Hall JG

3

1 reference

6 October 2017

Smith LJ

4

1 reference

6 October 2017

Berry AC

5

1 reference

6 October 2017

language of work or name

English

0 references

publication date

1 October 1991

1 reference

Journal of Medical Genetics

6 October 2017

1 reference

6 October 2017

28

1 reference

6 October 2017

10

1 reference

6 October 2017

701-703

1 reference

The distal arthrogryposes: delineation of new entities--review and nosologic discussion

6 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017058

In utero movement and use of limbs are necessary for normal growth: a study of individuals with arthrogryposis

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017058

A recessive form of congenital contractures and torticollis associated with malignant hyperthermia

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017058

Camptodactyly, cleft palate, and club foot (the Gordon syndrome). A report of a large pedigree

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017058

Congenital contractural arachnodactyly. A heritable disorder of connective tissue

6 June 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/1941966

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1136/JMG.28.10.701

1 reference

6 October 2017

1 reference

6 October 2017

PubMed publication ID

1941966

1 reference