(Q40238312)

English

Oligodactyly and multiple synostoses of the extremities: two cases in sibs. A variant of Cenani-Lenz syndactyly

scientific article published on April 1979

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

18 September 2017

Oligodactyly and multiple synostoses of the extremities: two cases in sibs. A variant of Cenani-Lenz syndactyly (English)

1 reference

Europe PubMed Central

PubMed publication ID

18 September 2017

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author name string

P Dodinval

1

1 reference

Europe PubMed Central

PubMed publication ID

18 September 2017

language of work or name

1 reference

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publication date

1 April 1979

1 reference

Europe PubMed Central

PubMed publication ID

18 September 2017

1 reference

Europe PubMed Central

PubMed publication ID

18 September 2017

48

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Europe PubMed Central

PubMed publication ID

18 September 2017

2

1 reference

Europe PubMed Central

PubMed publication ID

18 September 2017

183-189

1 reference

Europe PubMed Central

PubMed publication ID

18 September 2017

Split-hand and split-foot deformity inherited as an autosomal recessive trait

1 reference

https://pubmed.ncbi.nlm.nih.gov/222668

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Observation of a coarse malformation of the hand in the first generation & a bilateral radio-ulnar synostosis in the second one]

1 reference

https://pubmed.ncbi.nlm.nih.gov/222668

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Radioulnar synostosis, behavioral disturbance, and XYY chromosomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/222668

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital fusion of bones: Radiology, embryology and pathogenesis

1 reference

https://pubmed.ncbi.nlm.nih.gov/222668

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[The oligodactylia syndrome in human and its parallel mutation in the house mouse; an abnormality complex with ulnar aplasia, reduction of the ulnar marginal rays and anomalies of the intermaxillary bone, sternum, kidneys and spleen]

1 reference

https://pubmed.ncbi.nlm.nih.gov/222668

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The genetics of hand malformations

1 reference

https://pubmed.ncbi.nlm.nih.gov/222668

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial radioulnar synostosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/222668

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Limb anomalies in chromosomal aberrations

1 reference

https://pubmed.ncbi.nlm.nih.gov/222668

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital radio-ulnar synostosis. Report of 37 cases

1 reference

https://pubmed.ncbi.nlm.nih.gov/222668

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Total syndactylia and total radioulnar synostosis in 2 brothers. A contribution on the genetics of syndactylia

1 reference

https://pubmed.ncbi.nlm.nih.gov/222668

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Total syndactylism with mesomelic shortening of the arm, radioulnar and metacarpal synostoses and disorganization of the phalanges ("cenani syndactylism") (author's transl)

1 reference

https://pubmed.ncbi.nlm.nih.gov/222668

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00286902

1 reference

Europe PubMed Central

PubMed publication ID

18 September 2017

Dimensions Publication ID

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

18 September 2017

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