(Q50607626)

English

The Saethre-Chotzen syndrome with partial bifid of the distal phalanges of the great toes. Observations of three cases in one family.

scientific article published in January 1980

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scholarly article

1 reference

Europe PubMed Central

16 March 2018

http://europepmc.org/abstract/MED/7450776

The Saethre-Chotzen syndrome with partial bifid of the distal phalanges of the great toes. Observations of three cases in one family. (English)

1 reference

Europe PubMed Central

16 March 2018

http://europepmc.org/abstract/MED/7450776

Saethre-Chotzen syndrome

1 reference

based on heuristic

inferred from title

author name string

Z Kopyść

1

1 reference

Europe PubMed Central

16 March 2018

http://europepmc.org/abstract/MED/7450776

M Stańska

2

1 reference

Europe PubMed Central

16 March 2018

http://europepmc.org/abstract/MED/7450776

J Ryzko

3

1 reference

Europe PubMed Central

16 March 2018

http://europepmc.org/abstract/MED/7450776

B Kulczyk

4

1 reference

Europe PubMed Central

16 March 2018

http://europepmc.org/abstract/MED/7450776

publication date

1 January 1980

1 reference

Europe PubMed Central

16 March 2018

http://europepmc.org/abstract/MED/7450776

1 reference

Europe PubMed Central

16 March 2018

http://europepmc.org/abstract/MED/7450776

56

1 reference

Europe PubMed Central

16 March 2018

http://europepmc.org/abstract/MED/7450776

195-204

1 reference

Europe PubMed Central

16 March 2018

http://europepmc.org/abstract/MED/7450776

2

1 reference

Europe PubMed Central

16 March 2018

http://europepmc.org/abstract/MED/7450776

https://scigraph.springernature.com/pub.10.1007/bf00295694

0 references

Treacher Collins syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/7450776

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Acrocephalosyndactyly type 3: Chotzen's syndrome.

1 reference

https://pubmed.ncbi.nlm.nih.gov/7450776

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

1 reference

https://pubmed.ncbi.nlm.nih.gov/7450776

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Acrocephalosyndactylia associated with a chromosomal translocation. 46,XX, t (2p-; Cq+)

1 reference

https://pubmed.ncbi.nlm.nih.gov/7450776

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Saethre-Chotzen syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/7450776

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Craniosynostosis and craniosynostosis syndromes

1 reference

https://pubmed.ncbi.nlm.nih.gov/7450776

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Incomplete Crouson disease or pseudo-Crouzon disease in a family]

1 reference

https://pubmed.ncbi.nlm.nih.gov/7450776

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Crouzon-Apert syndrome (dysostosis craniodigito-facialis)]

1 reference

https://pubmed.ncbi.nlm.nih.gov/7450776

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[A case of Crouzon-Apert syndrome.]

1 reference

https://pubmed.ncbi.nlm.nih.gov/7450776

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Apert's syndrome (a type of acrocephalosyndactyly)-observations on a British series of thirty-nine cases

1 reference

https://pubmed.ncbi.nlm.nih.gov/7450776

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Saethre-Chotzen syndrome.

1 reference

https://pubmed.ncbi.nlm.nih.gov/7450776

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The hand and Apert's syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/7450776

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

On the classification of the acrocephalosyndactyly syndromes

1 reference

https://pubmed.ncbi.nlm.nih.gov/7450776

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An etiologic and nosologic overview of craniosynostosis syndromes

1 reference

https://pubmed.ncbi.nlm.nih.gov/7450776

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Acrocephalosyndactyly--Apert's Syndrome]

1 reference

https://pubmed.ncbi.nlm.nih.gov/7450776

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Apert's syndrome (acrocephalosyndactylia) in a 6-year-old girl

1 reference

https://pubmed.ncbi.nlm.nih.gov/7450776

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Apert's acrocephalosyndactyly in mother and daughter: cleft palate in the mother

1 reference

https://pubmed.ncbi.nlm.nih.gov/7450776

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

1 reference

https://pubmed.ncbi.nlm.nih.gov/7450776

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

DOMINANT HEREDITARY ACROCEPHALOSYNDACTYLIA

1 reference

https://pubmed.ncbi.nlm.nih.gov/7450776

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Acrocephalosyndactyly, or apert's syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/7450776

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00295694

1 reference

Europe PubMed Central

16 March 2018

http://europepmc.org/abstract/MED/7450776

1 reference

Europe PubMed Central

16 March 2018

http://europepmc.org/abstract/MED/7450776

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