(Q68467371)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3402993%20AND%20SRC:MED&resulttype=core&format=json

24 September 2019

title

Linkage analysis using multiple DNA polymorphic markers in normal families and in families with fragile X syndrome (English)

1 reference

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24 September 2019

1 reference

S N Thibodeau

1

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24 September 2019

H R Dorkins

2

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24 September 2019

K R Faulk

3

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24 September 2019

R Berry

4

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24 September 2019

A C Smith

5

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24 September 2019

R Hagerman

6

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24 September 2019

A King

7

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24 September 2019

K E Davies

8

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24 September 2019

publication date

1 July 1988

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24 September 2019

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3402993%20AND%20SRC:MED&resulttype=core&format=json

24 September 2019

volume

79

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24 September 2019

issue

3

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24 September 2019

page(s)

219-227

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https://scigraph.springernature.com/pub.10.1007/bf00366240

24 September 2019

exact match

0 references

cites work

Cognitive profiles and the spectrum of clinical manifestations in heterozygous fra (X) females.

1 reference

12 December 2020

The genetic linkage map of the human X chromosome

1 reference

12 December 2020

Gene organization and recombinational hotspots in the murine major histocompatibility complex

1 reference

12 December 2020

Hypothesis regarding the nature of the fragile X mutation. A reply to Winter and Pembrey

1 reference

12 December 2020

Further segregation analysis of the fragile X syndrome with special reference to transmitting males

1 reference

12 December 2020

Labeling deoxyribonucleic acid to high specific activity in vitro by nick translation with DNA polymerase I

1 reference

12 December 2020

Genetic linkage heterogeneity in the fragile X syndrome

1 reference

12 December 2020

Fragile X syndrome: a unique mutation in man.

1 reference

12 December 2020

Report of the Committee on Methods of Linkage Analysis and Reporting

1 reference

12 December 2020

Linkage and recombination between fragile X-linked mental retardation and the factor IX gene.

1 reference

12 December 2020

Detection of specific sequences among DNA fragments separated by gel electrophoresis

1 reference

12 December 2020

Linkage analysis and family classification under heterogeneity

1 reference

12 December 2020

Ten families with fragile X syndrome: linkage relationships with four DNA probes from distal Xq

1 reference

12 December 2020

Recombination and amplification of pyrimidine-rich sequences may be responsible for initiation and progression of the Xq27 fragile site: an hypothesis

1 reference

12 December 2020

A cytological map of the human X chromosome--evidence for non-random recombination

1 reference

12 December 2020

Evidence against close linkage of the loci for fraXq of Martin-Bell syndrome and for factor IX

1 reference

12 December 2020

Genetic analysis of the fragile-X mental retardation syndrome with two flanking polymorphic DNA markers

1 reference

12 December 2020

Linkage analysis using multiple Xq DNA polymorphisms in normal families, families with the fragile X syndrome, and other families with X linked conditions

1 reference

12 December 2020

Genetic heterogeneity of X-linked mental retardation with fragile X. Association of tight linkage to factor IX and incomplete penetrance in males.

1 reference

12 December 2020

Linkage analysis of X-linked mental retardation with and without fragile-X using factor IX gene probe

1 reference

12 December 2020

Further evidence for genetic heterogeneity in the fragile X syndrome.

1 reference

12 December 2020

DNA linkage studies in the fragile X syndrome suggest genetic heterogeneity

1 reference

12 December 2020

Close linkage of fragile X-mental retardation syndrome to haemophilia B and transmission through a normal male

1 reference

12 December 2020

RFLP for linkage analysis of fragile X syndrome

1 reference

12 December 2020

Mapping of DNA markers close to the fragile site on the human X chromosome at Xq27.3.

1 reference

12 December 2020

Easy calculations of lod scores and genetic risks on small computers

1 reference

12 December 2020

Phenotypic variation in male-transmitted fragile X: genetic inferences.

1 reference

12 December 2020

Linkage studies of X-linked mental retardation: high frequency of recombination in the telomeric region of the human X chromosome (fragile site/linkage/recombination/X chromosome).

1 reference

12 December 2020

Two anonymous X-specific human sequences detecting restriction fragment length polymorphisms in region Xq26?qter

1 reference

12 December 2020

The fragile X syndrome in a large family. III. Investigations on linkage of flanking DNA markers with the fragile site Xq27.

1 reference

12 December 2020

The genetic distance between the coagulation factor IX gene and the locus for the fragile X syndrome: clinical implications

1 reference

12 December 2020

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

1 reference

12 December 2020

Isolation and characterization of a cDNA coding for human factor IX

1 reference

12 December 2020

Genetic mapping of the human X chromosome by using restriction fragment length polymorphisms

1 reference

12 December 2020

Analysis of linkage relationships between genetic markers around the fragile X locus with special reference to the daughters of normal transmitting males

1 reference

12 December 2020

Linkage and genetic counselling for the fragile X using DNA probes 52A, F9, DX13, and ST14

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00366240

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3402993%20AND%20SRC:MED&resulttype=core&format=json

24 September 2019

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