(Q35562927)

English

Recessive omodysplasia: five new cases and review of the literature

scientific article published on 18 October 2003

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

1 reference

Europe PubMed Central

Recessive omodysplasia: five new cases and review of the literature (English)

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

Andrew Oliver Mungo Wilkie

3

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

Memnune Yüksel-Apak

4

object named as

Memune Yüksel-Apak

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

author name string

Nursel H Elçioglu

1

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

Karl H Gustavson

2

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

Jürgen W Spranger

5

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

publication date

18 October 2003

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

Pediatric Radiology

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

34

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

1

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

75-82

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

A New Dwarfing Syndrome with Extreme Shortening of Humeri and Severe Coxa Vara

1 reference

https://pubmed.ncbi.nlm.nih.gov/14566439

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Rhizomelic bone dysplasia with club-like femora. A distinctive, easily recognisable disease. Case report.

1 reference

https://pubmed.ncbi.nlm.nih.gov/14566439

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Bilateral humerus varus; with report of a case

1 reference

https://pubmed.ncbi.nlm.nih.gov/14566439

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A new skeletal dysplasia syndrome with rhizomelia of the humeri and other malformations

1 reference

https://pubmed.ncbi.nlm.nih.gov/14566439

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

DIASTROPHIC DWARFISM IN EARLY INFANCY

1 reference

https://pubmed.ncbi.nlm.nih.gov/14566439

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Nosology of omodysplasia.

1 reference

https://pubmed.ncbi.nlm.nih.gov/14566439

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial rhizomelic dysplasia: phenotypic variation or heterogeneity?

1 reference

https://pubmed.ncbi.nlm.nih.gov/14566439

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Long-term follow-up of two sibs with Larsen syndrome possibly due to parental germ-line mosaicism

1 reference

https://pubmed.ncbi.nlm.nih.gov/14566439

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autosomal recessive omodysplasia.

1 reference

https://pubmed.ncbi.nlm.nih.gov/14566439

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital distal humeral dysplasia: a case report.

1 reference

https://pubmed.ncbi.nlm.nih.gov/14566439

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

1 reference

https://pubmed.ncbi.nlm.nih.gov/14566439

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autosomal recessive omodysplasia

1 reference

https://pubmed.ncbi.nlm.nih.gov/14566439

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autosomal recessive omodysplasia: report of three additional cases

1 reference

https://pubmed.ncbi.nlm.nih.gov/14566439

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Parental consanguinity in two sibs with omodysplasia

1 reference

https://pubmed.ncbi.nlm.nih.gov/14566439

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Rhizomelic Bone Dysplasia with Club-like Femora (Case report and confirmation of a syndrome)

1 reference

https://pubmed.ncbi.nlm.nih.gov/14566439

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Symmetrical shortening of both humeri (author's transl)

1 reference

https://pubmed.ncbi.nlm.nih.gov/14566439

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Atelosteogenesis type III: a distinct skeletal dysplasia with features overlapping atelosteogenesis and oto-palato-digital syndrome type II.

1 reference

https://pubmed.ncbi.nlm.nih.gov/14566439

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Humero-Spinal Dysostosis With Congenital Heart Disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/14566439

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Atelosteogenesis syndromes: a review, with comments on their pathogenesis

1 reference

https://pubmed.ncbi.nlm.nih.gov/14566439

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autosomal-recessive omodysplasia: prenatal diagnosis and histomorphometric assessment of the physeal plates of the long bones

1 reference

https://pubmed.ncbi.nlm.nih.gov/14566439

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial congenital micromelic dysplasia with dislocation of radius and distinct face: a new skeletal dysplasia syndrome.

1 reference

https://pubmed.ncbi.nlm.nih.gov/14566439

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A new syndrome. Short limbs, abnormal facial appearance, and congenital heart defect

1 reference

https://pubmed.ncbi.nlm.nih.gov/14566439

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Omodysplasia: an affected mother and son.

1 reference

https://pubmed.ncbi.nlm.nih.gov/14566439

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00247-003-1064-9

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

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