(Q38326364)

2 September 2017

title

Polymerase chain reaction analysis of fragile X mutations (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1427787

25 September 2022

author name string

S. H. Erster

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1427787

25 September 2022

W. T. Brown

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1427787

25 September 2022

P. Goonewardena

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1427787

25 September 2022

C. S. Dobkin

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1427787

25 September 2022

E. C. Jenkins

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1427787

25 September 2022

R. G. Pergolizzi

6

1 reference

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25 September 2022

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=1427787

25 September 2022

publication date

1 September 1992

1 reference

2 September 2017

1 reference

2 September 2017

volume

90

1 reference

2 September 2017

issue

1-2

1 reference

2 September 2017

page(s)

55-61

1 reference

Molecular cloning and analysis of the fragile X region in man

2 September 2017

cites work

1 reference

12 December 2020

Further evidence for genetic heterogeneity in the fragile X syndrome.

1 reference

12 December 2020

Prenatally detected fragile X females: Long-term follow-up studies show high risk of mental impairment

1 reference

12 December 2020

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

1 reference

12 December 2020

Analysis of human Y-chromosome-specific reiterated DNA in chromosome variants

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Ethidium bromide does not fluoresce when intercalated adjacent to 7-deazaguanine in duplex DNA

1 reference

12 December 2020

The fragile X: progress toward solving the puzzle

1 reference

12 December 2020

Structure-independent DNA amplification by PCR using 7-deaza-2'-deoxyguanosine

1 reference

12 December 2020

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

1 reference

12 December 2020

Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox

1 reference

12 December 2020

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

1 reference

12 December 2020

Recent experience in prenatal fra(X) detection

1 reference

12 December 2020

PCR-based detection of a polymorphic BamHI site in intron 1 of the human retinoblastoma (RB) gene

1 reference

12 December 2020

DNA sequencing with Thermus aquaticus DNA polymerase and direct sequencing of polymerase chain reaction-amplified DNA

1 reference

12 December 2020

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

1 reference

12 December 2020

Conference report: International Workshop on the fragile X and X-linked mental retardation.

1 reference

12 December 2020

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

1 reference

12 December 2020

Poly(7-deazaguanylic acid), the homopolynucleotide of the parent nucleoside of queuosine

1 reference

12 December 2020

An improved method for prenatal diagnosis of genetic diseases by analysis of amplified DNA sequences. Application to hemophilia A.

1 reference

12 December 2020

X-Linked mental retardation with macro-orchidism and the fragile site at Xq27 or 28

1 reference

12 December 2020

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

1 reference

12 December 2020

Fragile X genotype characterized by an unstable region of DNA.

1 reference

12 December 2020

Progress toward an internal control system for fragile-X induction by 5-fluorodeoxyuridine in whole-blood cultures.

1 reference

12 December 2020

Organic solvents as facilitators of polymerase chain reaction

1 reference

12 December 2020

Detection of full fragile X mutation.

1 reference

12 December 2020

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

1 reference

12 December 2020

Isolation of a human DNA sequence which spans the fragile X.

1 reference

12 December 2020

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

1 reference

12 December 2020

Direct cloning and sequence analysis of enzymatically amplified genomic sequences

1 reference

12 December 2020

Direct diagnosis by DNA analysis of the fragile X syndrome of mental retardation

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00210744

1 reference

Dimensions Publication ID

2 September 2017

1034678910

0 references

1 reference