(Q34207831)

English

Studies of malformation syndromes of man 33: the FG syndrome. An X-linked recessive syndrome of multiple congenital anomalies and mental retardation.

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scholarly article

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4365204%20AND%20SRC:MED&resulttype=core&format=json

26 September 2019

Studies of malformation syndromes of man 33: the FG syndrome. An X-linked recessive syndrome of multiple congenital anomalies and mental retardation (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4365204%20AND%20SRC:MED&resulttype=core&format=json

26 September 2019

congenital disorder

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John Marius Opitz

1

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Opitz JM

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Europe PubMed Central

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26 September 2019

author name string

Kaveggia EG

2

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Europe PubMed Central

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26 September 2019

publication date

1 April 1974

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Europe PubMed Central

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26 September 2019

Zeitschrift fur Kinderheilkunde

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Europe PubMed Central

PubMed publication ID

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26 September 2019

117

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Europe PubMed Central

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26 September 2019

1

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Europe PubMed Central

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26 September 2019

1-18

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Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4365204%20AND%20SRC:MED&resulttype=core&format=json

26 September 2019

Congenital absence of the corpus callosum; report of a case and review of the literature

1 reference

https://pubmed.ncbi.nlm.nih.gov/4365204

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Agenesis of the corpus callosum.]

1 reference

https://pubmed.ncbi.nlm.nih.gov/4365204

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mid-line anomalies of the brain; their diagnosis by pneumoencephalography.

1 reference

https://pubmed.ncbi.nlm.nih.gov/4365204

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Agenesis of the corpus callosum; a report of two cases in siblings.

1 reference

https://pubmed.ncbi.nlm.nih.gov/4365204

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Agenesis of the corpus callosum with concomitant malformations, including atresia of the foramens of Luschka and Magendie.

1 reference

https://pubmed.ncbi.nlm.nih.gov/4365204

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Agenesis of the corpus callosum; a study of 18 cases diagnosed during life.

1 reference

https://pubmed.ncbi.nlm.nih.gov/4365204

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Agenesis of the corpus callosum diagnosed during life; review of the literature and presentation of two cases.

1 reference

https://pubmed.ncbi.nlm.nih.gov/4365204

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

SEX-LINKED IMPERFORATE ANUS

1 reference

https://pubmed.ncbi.nlm.nih.gov/4365204

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Agenesis of the corpus callosum in two sisters

1 reference

https://pubmed.ncbi.nlm.nih.gov/4365204

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Malignant familial early infantile convulsive disoders, partial relation with aplasia of corpus callosum.]

1 reference

https://pubmed.ncbi.nlm.nih.gov/4365204

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Agenesis of the corpus callosum and associated malformations.

1 reference

https://pubmed.ncbi.nlm.nih.gov/4365204

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

HEREDITARY PARTIAL AGENESIS OF CORPUS CALLOSUM; BIOCHEMICAL AND PATHOLOGICAL STUDIES.

1 reference

https://pubmed.ncbi.nlm.nih.gov/4365204

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4365204%20AND%20SRC:MED&resulttype=core&format=json

26 September 2019

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