(Q35434440)

8 August 2017

title

Clinical and radiological assessment of a family with mild brachydactyly type A1: the usefulness of metacarpophalangeal profiles (English)

1 reference

8 August 2017

main subject

brachydactyly type A1

1 reference

Armour CM

1

1 reference

8 August 2017

Bulman DE

series ordinal

2

1 reference

8 August 2017

Hunter AG

series ordinal

3

1 reference

8 August 2017

language of work or name

English

0 references

publication date

1 April 2000

1 reference

Journal of Medical Genetics

8 August 2017

published in

1 reference

8 August 2017

volume

37

1 reference

8 August 2017

issue

4

1 reference

8 August 2017

page(s)

292-296

1 reference

Evaluation of candidate genes for familial brachydactyly

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=1734558

Metacarpophalangeal Length in the Evaluation of Skeletal Malformation

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734558

Metacarpophalangeal pattern profiles in the evaluation of skeletal malformations.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734558

Type A1 brachydactyly, dwarfism, ptosis, mixed partial hearing loss, microcephaly, and mental retardation

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734558

Classification and identification of inherited brachydactylies

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734558

Brachydactyly type A1 with abnormal menisci and scoliosis in three generations

12 July 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/10745048

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

De novo apparently balanced reciprocal translocation between 5q1l.2 and 17q23 associated with Klippel‐Feil anomaly and type A1 brachydactyly

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/10745048

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

A boy with severe manifestations of type A1 brachydactyly

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/10745048

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1136/JMG.37.4.292

1 reference

8 August 2017

1 reference

8 August 2017

1 reference