(Q69217845)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3623561%20AND%20SRC:MED&resulttype=core&format=json

30 September 2019

title

Prevalence of the fragile X syndrome in four birth cohorts of children of school age (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3623561%20AND%20SRC:MED&resulttype=core&format=json

30 September 2019

1 reference

M Kähkönen

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3623561%20AND%20SRC:MED&resulttype=core&format=json

30 September 2019

T Alitalo

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3623561%20AND%20SRC:MED&resulttype=core&format=json

30 September 2019

E Airaksinen

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3623561%20AND%20SRC:MED&resulttype=core&format=json

30 September 2019

R Matilainen

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3623561%20AND%20SRC:MED&resulttype=core&format=json

30 September 2019

K Launiala

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3623561%20AND%20SRC:MED&resulttype=core&format=json

30 September 2019

S Autio

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3623561%20AND%20SRC:MED&resulttype=core&format=json

30 September 2019

J Leisti

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3623561%20AND%20SRC:MED&resulttype=core&format=json

30 September 2019

publication date

1 September 1987

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3623561%20AND%20SRC:MED&resulttype=core&format=json

30 September 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3623561%20AND%20SRC:MED&resulttype=core&format=json

30 September 2019

volume

77

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3623561%20AND%20SRC:MED&resulttype=core&format=json

30 September 2019

issue

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3623561%20AND%20SRC:MED&resulttype=core&format=json

30 September 2019

page(s)

85-87

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3623561%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1007/bf00284720

30 September 2019

exact match

0 references

cites work

Screening for fra(X)(q) in a population of mentally retarded males.

1 reference

12 December 2020

The marker (X) syndrome: a cytogenetic and genetic analysis.

1 reference

12 December 2020

The diagnosis and frequency of X-linked conditions in a cohort of moderately retarded males with affected brothers

1 reference

12 December 2020

Population incidence and segregation ratios in the Martin-Bell syndrome.

1 reference

12 December 2020

Frequency of rare fragile sites among mentally subnormal schoolchildren

1 reference

12 December 2020

Heterozygous expression of X-linked mental retardation and X-chromosome marker fra(X)(q27).

1 reference

12 December 2020

The frequency of the fragile X chromosome among schoolchildren in Coventry

1 reference

12 December 2020

Marker X-associated mental retardation. A study of 150 retarded males.

1 reference

12 December 2020

Preventive screening for the fragile X syndrome

1 reference

12 December 2020

Marker (X)-Linked Mental Retardation

1 reference

12 December 2020

Fragile X syndrome in mildly mentally retarded children in a northern Swedish county. A prevalence study.

1 reference

12 December 2020

Studies of the fragile (X) syndrome in populations of mentally retarded individuals in Hawaii

1 reference

12 December 2020

Prevalence of the fragile-X syndrome in mentally retarded boys in a Swedish county.

1 reference

12 December 2020

Heritable fragile sites on human chromosomes. XII. Population cytogenetics

1 reference

12 December 2020

The fragile X syndrome. A study of 83 families.

1 reference

12 December 2020

A cytogenetic study of a population of retarded females with special reference to the fragile (X) syndrome

1 reference

12 December 2020