(Q57264019)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2995232%20AND%20SRC:MED&resulttype=core&format=json

8 October 2019

title

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

1 reference

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8 October 2019

1 reference

4

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8 October 2019

author name string

B Zoll

1

1 reference

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8 October 2019

J Arnemann

2

1 reference

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8 October 2019

M Krawczak

3

1 reference

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8 October 2019

G Pescia

5

1 reference

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8 October 2019

W Wahli

6

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8 October 2019

P Steinbach

7

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8 October 2019

J Schmidtke

8

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8 October 2019

publication date

1 January 1985

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8 October 2019

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8 October 2019

volume

71

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8 October 2019

issue

2

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8 October 2019

page(s)

122-126

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X-linked mental retardation with fragile X. A pedigree showing transmission by apparently unaffected males and partial expression in female carriers

8 October 2019

cites work

1 reference

12 December 2020

Heritable fragile sites on human chromosomes. VIII. Preliminary population cytogenetic data on the folic-acid-sensitive fragile sites

1 reference

12 December 2020

On the frequency of telomeric chromosomal changes induced by culture conditions suitable for fragile X expression

1 reference

12 December 2020

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

1 reference

12 December 2020

Prenatal diagnosis of X-linked mental retardation with fragile (X) using fetoscopy and fetal blood sampling

1 reference

12 December 2020

Transmission of fragile (X) (q27) site from a male

1 reference

12 December 2020

The fragile X syndrome: the patients and their chromosomes

1 reference

12 December 2020

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

1 reference

12 December 2020

Molecular cloning of the gene for human anti-haemophilic factor IX.

1 reference

12 December 2020

Regional localization on the human X chromosome and polymorphism of the coagulation factor IX gene (hemophilia B locus).

1 reference

12 December 2020

Sequential tests for the detection of linkage

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

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

1 reference

12 December 2020

Enzymatic synthesis of deoxyribonucleic acid. XXXII. Replication of duplex deoxyribonucleic acid by polymerase at a single strand break

1 reference

12 December 2020

Feasibility of fragile X chromosome prenatal diagnosis demonstrated

1 reference

12 December 2020

Recombinant DNA approach to X-linked mental retardation

1 reference

12 December 2020

Detection of specific sequences among DNA fragments separated by gel electrophoresis

1 reference

12 December 2020

Prenatal detection of a fetus hemizygous for the fragile X-chromosome

1 reference

12 December 2020

Tables for the cytogenetic study of fragile X chromosomes for diagnostic purposes

1 reference

12 December 2020

Fragile sites in human chromosomes II: demonstration of the fragile site Xq27 in carriers of X-linked mental retardation

1 reference

12 December 2020

Restriction fragment length polymorphisms at the human parathyroid hormone gene locus

1 reference

12 December 2020

Marker (X)-Linked Mental Retardation

1 reference

12 December 2020

Nonspecific X-linked mental retardation--a review

1 reference

12 December 2020

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

1 reference

12 December 2020

A PEDIGREE OF MENTAL DEFECT SHOWING SEX-LINKAGE.

1 reference

12 December 2020

Transmission of the marker X syndrome trait by unaffected males: conclusions from studies of large families

1 reference

12 December 2020

Characterisation and use of an intragenic polymorphic marker for detection of carriers of haemophilia B (factor IX deficiency).

1 reference

12 December 2020

Transmission of fragile (X)(q27) from normal male(s)

1 reference

12 December 2020

Fragile X trait in a large kindred: transmission also through normal males

1 reference

12 December 2020

Heritable fragile sites on human chromosomes. III. Detection of fra(X)(q27) in males with X-linked mental retardation and in their female relatives

1 reference

12 December 2020

The gene structure of human anti-haemophilic factor IX.

1 reference

12 December 2020

A marker X chromosome

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

Identifiers

DOI

10.1007/BF00283366

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2995232%20AND%20SRC:MED&resulttype=core&format=json

8 October 2019

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