(Q28235115)

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17 November 2022

3

A. Pizzuti

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17 November 2022

author name string

Y. H. Fu

1

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17 November 2022

D. P. Kuhl

2

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17 November 2022

M. Pieretti

4

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17 November 2022

J. S. Sutcliffe

5

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17 November 2022

S. Richards

6

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17 November 2022

A. J. Verkerk

7

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17 November 2022

J. J. Holden

8

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17 November 2022

R. G. Fenwick

9

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17 November 2022

S. T. Warren

10

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full work available at URL

17 November 2022

language of work or name

English

0 references

publication date

20 December 1991

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https://api.elsevier.com/content/article/PII:0092867491902835?httpAccept=text/xml

1 reference

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https://api.elsevier.com/content/article/PII:0092867491902835?httpAccept=text/plain

17 November 2022

1 reference

https://api.crossref.org/works/10.1016/0092-8674(91)90283-5

17 November 2022

0 references

67

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issue

6

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page(s)

1047-58

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cites work

Physical mapping across the fragile X: hypermethylation and clinical expression of the fragile X syndrome

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Random cloning and sequencing by the M13/dideoxynucleotide chain termination method.

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Molecular cloning and analysis of the fragile X region in man

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The CEPH consortium linkage map of human chromosome 1

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

17 November 2022

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Isolation of sequences that span the fragile X and identification of a fragile X-related CpG island

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Hypervariable 'minisatellite' regions in human DNA.

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Spontaneous mutation rates to new length alleles at tandem-repetitive hypervariable loci in human DNA.

17 November 2022

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Mapping of DNA instability at the fragile X to a trinucleotide repeat sequence p(CCG)n

17 November 2022

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Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndrome

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Absence of expression of the FMR-1 gene in fragile X syndrome

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

17 November 2022

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

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17 November 2022

Gene amplification

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Characterization and expression of a cDNA encoding the human androgen receptor

17 November 2022

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Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome

17 November 2022

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Abnormal pattern detected in fragile-X patients by pulsed-field gel electrophoresis

17 November 2022

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

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Fragile X genotype characterized by an unstable region of DNA.

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