(Q52291816)

English

The Weaver syndrome: a rare type of primordial overgrowth.

scientific article published in November 1981

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Statements

scholarly article

1 reference

Europe PubMed Central

28 April 2018

http://europepmc.org/abstract/MED/7318839

The Weaver syndrome: a rare type of primordial overgrowth. (English)

1 reference

Europe PubMed Central

28 April 2018

http://europepmc.org/abstract/MED/7318839

Weaver syndrome

1 reference

based on heuristic

inferred from title

author name string

F Majewski

1

1 reference

Europe PubMed Central

28 April 2018

http://europepmc.org/abstract/MED/7318839

M Ranke

2

1 reference

Europe PubMed Central

28 April 2018

http://europepmc.org/abstract/MED/7318839

H Kemperdick

3

1 reference

Europe PubMed Central

28 April 2018

http://europepmc.org/abstract/MED/7318839

E Schmidt

4

1 reference

Europe PubMed Central

28 April 2018

http://europepmc.org/abstract/MED/7318839

publication date

1 November 1981

1 reference

Europe PubMed Central

28 April 2018

http://europepmc.org/abstract/MED/7318839

European Journal of Pediatrics

1 reference

Europe PubMed Central

28 April 2018

http://europepmc.org/abstract/MED/7318839

137

1 reference

Europe PubMed Central

28 April 2018

http://europepmc.org/abstract/MED/7318839

277-282

1 reference

Europe PubMed Central

28 April 2018

http://europepmc.org/abstract/MED/7318839

3

1 reference

Europe PubMed Central

28 April 2018

http://europepmc.org/abstract/MED/7318839

https://scigraph.springernature.com/pub.10.1007/bf00443257

0 references

[Cerebral gigantism in childhood]

1 reference

https://pubmed.ncbi.nlm.nih.gov/7318839

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Syndrome of accelerated skeletal maturation, type Marshall (author's transl)

1 reference

https://pubmed.ncbi.nlm.nih.gov/7318839

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A new overgrowth syndrome with accelerated skeletal maturation, unusual facies, and camptodactyly

1 reference

https://pubmed.ncbi.nlm.nih.gov/7318839

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Marshall-Smith syndrome with large bifrontal diameter, broad distal femora, camptodactly, and without broad middle phalanges

1 reference

https://pubmed.ncbi.nlm.nih.gov/7318839

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Studies of malformation syndromes of man XXIX: the Wiedemann-Beckwith syndrome. Clinical, genetic and pathogenetic studies of 12 cases

1 reference

https://pubmed.ncbi.nlm.nih.gov/7318839

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Benign familial macrocephaly: report of a family and review of the literature

1 reference

https://pubmed.ncbi.nlm.nih.gov/7318839

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00443257

1 reference

Europe PubMed Central

28 April 2018

http://europepmc.org/abstract/MED/7318839

1 reference

Europe PubMed Central

28 April 2018

http://europepmc.org/abstract/MED/7318839

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