(Q24517851)

English

FG syndrome

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

2 July 2017

FG syndrome (English)

1 reference

Europe PubMed Central

PubMed publication ID

2 July 2017

2

object named as

Baraitser M

author given names

M

author last names

Baraitser

1 reference

Europe PubMed Central

PubMed publication ID

2 July 2017

author name string

Thompson E

1

author given names

E

author last names

Thompson

1 reference

Europe PubMed Central

PubMed publication ID

2 July 2017

language of work or name

0 references

publication date

1 March 1987

1 reference

Europe PubMed Central

PubMed publication ID

2 July 2017

Journal of Medical Genetics

1 reference

Europe PubMed Central

PubMed publication ID

2 July 2017

24

1 reference

Europe PubMed Central

PubMed publication ID

2 July 2017

3

1 reference

Europe PubMed Central

PubMed publication ID

2 July 2017

139-143

1 reference

Europe PubMed Central

PubMed publication ID

2 July 2017

Two retarded male cousins with odd facies, hypotonia, and severe constipation: possible examples of the X linked FG syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049945

27 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049945

27 September 2017

The FG syndrome: 7 new cases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049945

27 September 2017

The FG syndrome: Further characterization, report of a third family, and of a sporadic case

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049945

27 September 2017

Studies of malformation syndromes of humans XXXIIIC: the FG syndrome - further studies on three affected individuals from the FG family

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049945

30 May 2018

Necropsy findings in a child with FG syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049945

30 May 2018

A new syndrome of mental deficiency with craniofacial, limb, and anal abnormalities

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049945

30 May 2018

Sensorineural deafness in the FG syndrome: report on four new cases

1 reference

https://pubmed.ncbi.nlm.nih.gov/3572995

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

FG syndrome in a premature male

1 reference

https://pubmed.ncbi.nlm.nih.gov/3572995

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://api.crossref.org/works/10.1136%2FJMG.24.3.139

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1136/JMG.24.3.139

0 references

release_fgbt4asbbfd6nft3euve35trbi

0 references

PMC publication ID

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

2 July 2017

ResearchGate publication ID

0 references

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